ENST00000695651.1:n.2646A>T
|
|
|
ENST00000695653.1:c.2207A>T
|
ENSP00000512084.1:p.Glu736Val
|
|
ENST00000695654.1:c.3323A>T
|
ENSP00000512085.1:p.Glu1108Val
|
|
ENST00000695689.1:c.269A>T
|
ENSP00000512101.1:n.269A>T
|
|
ENST00000695690.1:n.489A>T
|
|
|
ENST00000695691.1:n.489A>T
|
|
|
ENST00000245907.11:c.4298A>T
MANE Select
|
ENSP00000245907.4:p.Glu1433Val
|
|
ENST00000245907.10:c.4298A>T
|
ENSP00000245907.4:p.Glu1433Val
|
|
ENST00000596548.1:c.419A>T
|
ENSP00000469744.1:p.Glu140Val
|
|
ENST00000599899.5:n.1257A>T
|
|
|
ENST00000601008.1:c.242-4035A>T
|
ENSP00000471384.1:n.242-4035A>T
|
|
NM_000064.3:c.4298A>T
|
NP_000055.2:p.Glu1433Val
|
|
NM_000064.4:c.4298A>T
MANE Select
|
NP_000055.2:p.Glu1433Val
|
|