ENST00000695651.1:n.2809A>T
|
|
|
ENST00000695653.1:c.2370A>T
|
ENSP00000512084.1:p.Glu790Asp
|
|
ENST00000695654.1:c.3486A>T
|
ENSP00000512085.1:p.Glu1162Asp
|
|
ENST00000695689.1:c.432A>T
|
ENSP00000512101.1:n.432A>T
|
|
ENST00000695690.1:n.1526A>T
|
|
|
ENST00000695691.1:n.1322A>T
|
|
|
ENST00000245907.11:c.4461A>T
MANE Select
|
ENSP00000245907.4:p.Glu1487Asp
|
|
ENST00000245907.10:c.4461A>T
|
ENSP00000245907.4:p.Glu1487Asp
|
|
ENST00000599668.1:n.56A>T
|
|
|
ENST00000599899.5:n.1420A>T
|
|
|
ENST00000601008.1:c.242-1534A>T
|
ENSP00000471384.1:n.242-1534A>T
|
|
NM_000064.3:c.4461A>T
|
NP_000055.2:p.Glu1487Asp
|
|
NM_000064.4:c.4461A>T
MANE Select
|
NP_000055.2:p.Glu1487Asp
|
|