ENST00000695651.1:n.2082A>T
|
|
|
ENST00000695652.1:c.3611A>T
|
ENSP00000512083.1:p.Asp1204Val
|
|
ENST00000695653.1:c.1643A>T
|
ENSP00000512084.1:p.Asp548Val
|
|
ENST00000695654.1:c.2759A>T
|
ENSP00000512085.1:p.Asp920Val
|
|
ENST00000695655.1:c.2675A>T
|
ENSP00000512086.1:n.2675A>T
|
|
ENST00000695692.1:n.3098A>T
|
|
|
ENST00000245907.11:c.3734A>T
MANE Select
|
ENSP00000245907.4:p.Asp1245Val
|
|
ENST00000245907.10:c.3734A>T
|
ENSP00000245907.4:p.Asp1245Val
|
|
ENST00000596238.1:n.177A>T
|
|
|
ENST00000601008.1:c.241+546A>T
|
ENSP00000471384.1:n.241+546A>T
|
|
NM_000064.3:c.3734A>T
|
NP_000055.2:p.Asp1245Val
|
|
NM_000064.4:c.3734A>T
MANE Select
|
NP_000055.2:p.Asp1245Val
|
|