ENST00000695651.1:n.2875A>C
|
|
|
ENST00000695653.1:c.2436A>C
|
ENSP00000512084.1:p.Glu812Asp
|
|
ENST00000695654.1:c.3552A>C
|
ENSP00000512085.1:p.Glu1184Asp
|
|
ENST00000695689.1:c.498A>C
|
ENSP00000512101.1:n.498A>C
|
|
ENST00000695690.1:n.1592A>C
|
|
|
ENST00000695691.1:n.1388A>C
|
|
|
ENST00000245907.11:c.4527A>C
MANE Select
|
ENSP00000245907.4:p.Glu1509Asp
|
|
ENST00000245907.10:c.4527A>C
|
ENSP00000245907.4:p.Glu1509Asp
|
|
ENST00000599668.1:n.122A>C
|
|
|
ENST00000599899.5:n.1486A>C
|
|
|
ENST00000601008.1:c.242-1468A>C
|
ENSP00000471384.1:n.242-1468A>C
|
|
NM_000064.3:c.4527A>C
|
NP_000055.2:p.Glu1509Asp
|
|
NM_000064.4:c.4527A>C
MANE Select
|
NP_000055.2:p.Glu1509Asp
|
|