Transcript | cDNA | Protein | Consequence | Exon | Intron |
---|---|---|---|---|---|
ENST00000346198.4 | c.291+33966C>T | - | intron_variant | - | 4/6 |
ENST00000349937.2 | c.450+33966C>T | - | intron_variant | - | 4/7 |
ENST00000352065.5 | c.382-41435C>T | - | intron_variant | - | 3/14 |
ENST00000355717.4 | c.382-41435C>T | - | intron_variant | - | 3/12 |
ENST00000355995.4 | c.450+33966C>T | - | intron_variant | - | 4/14 |
ENST00000369395.1 | c.382-41435C>T | - | intron_variant | - | 3/7 |
ENST00000369397.4 | c.382-41435C>T | - | intron_variant | - | 3/13 |
ENST00000534894.1 | c.450+33966C>T | - | intron_variant | - | 4/14 |
ENST00000536810.1 | c.450+33966C>T | - | intron_variant | - | 4/13 |
ENST00000538897.1 | c.450+33966C>T | - | intron_variant | - | 4/13 |
ENST00000542695.1 | c.-531-41435C>T | - | intron_variant | - | 3/14 |
ENST00000543371.1 | c.450+33966C>T | - | intron_variant | - | 4/13 |
ENST00000545257.1 | c.450+33966C>T | - | intron_variant | - | 4/14 |
NM_001146274.2 | c.450+33966C>T | - | intron_variant | - | 4/13 |
NM_001146283.2 | c.382-41435C>T | - | intron_variant | - | 3/12 |
NM_001146284.2 | c.382-41435C>T | - | intron_variant | - | 3/12 |
NM_001146285.1 | c.382-41435C>T | - | intron_variant | - | 3/12 |
NM_001146286.2 | c.382-41435C>T | - | intron_variant | - | 3/11 |
NM_001198525.2 | c.382-41435C>T | - | intron_variant | - | 3/14 |
NM_001198526.2 | c.382-41435C>T | - | intron_variant | - | 3/12 |
NM_001198527.2 | c.382-41435C>T | - | intron_variant | - | 3/14 |
NM_001198528.2 | c.382-41435C>T | - | intron_variant | - | 3/14 |
NM_001198529.2 | c.382-41435C>T | - | intron_variant | - | 3/12 |
NM_001198530.1 | c.381+46983C>T | - | intron_variant | - | 3/10 |
NM_001198531.2 | c.450+33966C>T | - | intron_variant | - | 4/12 |
NM_001363501.1 | c.450+33966C>T | - | intron_variant | - | 4/13 |
NM_001367943.1 | c.450+33966C>T | - | intron_variant | - | 4/14 |
NM_030756.5 | c.382-41435C>T | - | intron_variant | - | 3/13 |