Transcript | cDNA | Protein | Consequence | Exon | Intron |
---|---|---|---|---|---|
ENST00000269305.4 | c.215C>G | p.Pro72Arg | missense_variant | 4/11 | - |
ENST00000359597.4 | c.215C>G | p.Pro72Arg | missense_variant | 3/9 | - |
ENST00000413465.2 | c.215C>G | p.Pro72Arg | missense_variant | 3/7 | - |
ENST00000420246.2 | c.215C>G | p.Pro72Arg | missense_variant | 4/12 | - |
ENST00000445888.2 | c.215C>G | p.Pro72Arg | missense_variant | 4/11 | - |
ENST00000455263.2 | c.215C>G | p.Pro72Arg | missense_variant | 4/12 | - |
ENST00000503591.1 | c.215C>G | p.Pro72Arg | missense_variant | 5/6 | - |
ENST00000505014.1 | n.471C>G | - | non_coding_transcript_exon_variant | 3/5 | - |
ENST00000508793.1 | c.215C>G | p.Pro72Arg | missense_variant | 4/5 | - |
ENST00000509690.1 | c.-21-918C>G | - | intron_variant | - | 1/5 |
ENST00000514944.1 | c.96+228C>G | - | intron_variant | - | 3/5 |
ENST00000604348.1 | c.215C>G | p.Pro72Arg | missense_variant | 4/5 | - |
NM_000546.5 | c.215C>G | p.Pro72Arg | missense_variant | 4/11 | - |
NM_001126112.2 | c.215C>G | p.Pro72Arg | missense_variant | 4/11 | - |
NM_001126113.2 | c.215C>G | p.Pro72Arg | missense_variant | 4/12 | - |
NM_001126114.2 | c.215C>G | p.Pro72Arg | missense_variant | 4/12 | - |
NM_001126118.1 | c.98C>G | p.Pro33Arg | missense_variant | 3/10 | - |
NM_001276695.2 | c.98C>G | p.Pro33Arg | missense_variant | 4/12 | - |
NM_001276696.2 | c.98C>G | p.Pro33Arg | missense_variant | 4/12 | - |
NM_001276760.2 | c.98C>G | p.Pro33Arg | missense_variant | 4/11 | - |
NM_001276761.2 | c.98C>G | p.Pro33Arg | missense_variant | 4/11 | - |