ENST00000695651.1:n.2949A>T
|
|
|
ENST00000695653.1:c.2510A>T
|
ENSP00000512084.1:p.Asp837Val
|
|
ENST00000695654.1:c.3626A>T
|
ENSP00000512085.1:p.Asp1209Val
|
|
ENST00000695689.1:c.572A>T
|
ENSP00000512101.1:n.572A>T
|
|
ENST00000695690.1:n.1666A>T
|
|
|
ENST00000695691.1:n.1462A>T
|
|
|
ENST00000245907.11:c.4601A>T
MANE Select
|
ENSP00000245907.4:p.Asp1534Val
|
|
ENST00000245907.10:c.4601A>T
|
ENSP00000245907.4:p.Asp1534Val
|
|
ENST00000599668.1:n.221A>T
|
|
|
ENST00000599899.5:n.1560A>T
|
|
|
ENST00000601008.1:c.242-1196A>T
|
ENSP00000471384.1:n.242-1196A>T
|
|
ENST00000602229.1:c.48A>T
|
|
|
NM_000064.3:c.4601A>T
|
NP_000055.2:p.Asp1534Val
|
|
NM_000064.4:c.4601A>T
MANE Select
|
NP_000055.2:p.Asp1534Val
|
|