ENST00000695651.1:n.2088A>T
|
|
|
ENST00000695652.1:c.3617A>T
|
ENSP00000512083.1:p.Asp1206Val
|
|
ENST00000695653.1:c.1649A>T
|
ENSP00000512084.1:p.Asp550Val
|
|
ENST00000695654.1:c.2765A>T
|
ENSP00000512085.1:p.Asp922Val
|
|
ENST00000695655.1:c.2681A>T
|
ENSP00000512086.1:n.2681A>T
|
|
ENST00000695692.1:n.3104A>T
|
|
|
ENST00000245907.11:c.3740A>T
MANE Select
|
ENSP00000245907.4:p.Asp1247Val
|
|
ENST00000245907.10:c.3740A>T
|
ENSP00000245907.4:p.Asp1247Val
|
|
ENST00000596238.1:n.183A>T
|
|
|
ENST00000601008.1:c.241+552A>T
|
ENSP00000471384.1:n.241+552A>T
|
|
NM_000064.3:c.3740A>T
|
NP_000055.2:p.Asp1247Val
|
|
NM_000064.4:c.3740A>T
MANE Select
|
NP_000055.2:p.Asp1247Val
|
|