ENST00000695651.1:n.2874A=
|
|
|
ENST00000695653.1:c.2435A=
|
ENSP00000512084.1:p.Glu812=
|
|
ENST00000695654.1:c.3551A=
|
ENSP00000512085.1:p.Glu1184=
|
|
ENST00000695689.1:c.497A=
|
ENSP00000512101.1:n.497A=
|
|
ENST00000695690.1:n.1591A=
|
|
|
ENST00000695691.1:n.1387A=
|
|
|
ENST00000245907.11:c.4526A=
MANE Select
|
ENSP00000245907.4:p.Glu1509=
|
|
ENST00000245907.10:c.4526A=
|
ENSP00000245907.4:p.Glu1509=
|
|
ENST00000599668.1:n.121A=
|
|
|
ENST00000599899.5:n.1485A=
|
|
|
ENST00000601008.1:c.242-1469A=
|
ENSP00000471384.1:n.242-1469A=
|
|
NM_000064.3:c.4526A=
|
NP_000055.2:p.Glu1509=
|
|
NM_000064.4:c.4526A=
MANE Select
|
NP_000055.2:p.Glu1509=
|
|