ENST00000695651.1:n.2976A>G
|
|
|
ENST00000695653.1:c.2537A>G
|
ENSP00000512084.1:p.Tyr846Cys
|
|
ENST00000695654.1:c.3653A>G
|
ENSP00000512085.1:p.Tyr1218Cys
|
|
ENST00000695689.1:c.599A>G
|
ENSP00000512101.1:n.599A>G
|
|
ENST00000695690.1:n.1693A>G
|
|
|
ENST00000695691.1:n.1489A>G
|
|
|
ENST00000245907.11:c.4628A>G
MANE Select
|
ENSP00000245907.4:p.Tyr1543Cys
|
|
ENST00000245907.10:c.4628A>G
|
ENSP00000245907.4:p.Tyr1543Cys
|
|
ENST00000599668.1:n.248A>G
|
|
|
ENST00000599899.5:n.1587A>G
|
|
|
ENST00000601008.1:c.242-1169A>G
|
ENSP00000471384.1:n.242-1169A>G
|
|
ENST00000602229.1:c.75A>G
|
|
|
NM_000064.3:c.4628A>G
|
NP_000055.2:p.Tyr1543Cys
|
|
NM_000064.4:c.4628A>G
MANE Select
|
NP_000055.2:p.Tyr1543Cys
|
|