ENST00000695651.1:n.2836A>C
|
|
|
ENST00000695653.1:c.2397A>C
|
ENSP00000512084.1:p.Glu799Asp
|
|
ENST00000695654.1:c.3513A>C
|
ENSP00000512085.1:p.Glu1171Asp
|
|
ENST00000695689.1:c.459A>C
|
ENSP00000512101.1:n.459A>C
|
|
ENST00000695690.1:n.1553A>C
|
|
|
ENST00000695691.1:n.1349A>C
|
|
|
ENST00000245907.11:c.4488A>C
MANE Select
|
ENSP00000245907.4:p.Glu1496Asp
|
|
ENST00000245907.10:c.4488A>C
|
ENSP00000245907.4:p.Glu1496Asp
|
|
ENST00000599668.1:n.83A>C
|
|
|
ENST00000599899.5:n.1447A>C
|
|
|
ENST00000601008.1:c.242-1507A>C
|
ENSP00000471384.1:n.242-1507A>C
|
|
NM_000064.3:c.4488A>C
|
NP_000055.2:p.Glu1496Asp
|
|
NM_000064.4:c.4488A>C
MANE Select
|
NP_000055.2:p.Glu1496Asp
|
|