ENST00000695651.1:n.2874A>T
|
|
|
ENST00000695653.1:c.2435A>T
|
ENSP00000512084.1:p.Glu812Val
|
|
ENST00000695654.1:c.3551A>T
|
ENSP00000512085.1:p.Glu1184Val
|
|
ENST00000695689.1:c.497A>T
|
ENSP00000512101.1:n.497A>T
|
|
ENST00000695690.1:n.1591A>T
|
|
|
ENST00000695691.1:n.1387A>T
|
|
|
ENST00000245907.11:c.4526A>T
MANE Select
|
ENSP00000245907.4:p.Glu1509Val
|
|
ENST00000245907.10:c.4526A>T
|
ENSP00000245907.4:p.Glu1509Val
|
|
ENST00000599668.1:n.121A>T
|
|
|
ENST00000599899.5:n.1485A>T
|
|
|
ENST00000601008.1:c.242-1469A>T
|
ENSP00000471384.1:n.242-1469A>T
|
|
NM_000064.3:c.4526A>T
|
NP_000055.2:p.Glu1509Val
|
|
NM_000064.4:c.4526A>T
MANE Select
|
NP_000055.2:p.Glu1509Val
|
|