ENST00000695651.1:n.2834G>C
|
|
|
ENST00000695653.1:c.2395G>C
|
ENSP00000512084.1:p.Glu799Gln
|
|
ENST00000695654.1:c.3511G>C
|
ENSP00000512085.1:p.Glu1171Gln
|
|
ENST00000695689.1:c.457G>C
|
ENSP00000512101.1:n.457G>C
|
|
ENST00000695690.1:n.1551G>C
|
|
|
ENST00000695691.1:n.1347G>C
|
|
|
ENST00000245907.11:c.4486G>C
MANE Select
|
ENSP00000245907.4:p.Glu1496Gln
|
|
ENST00000245907.10:c.4486G>C
|
ENSP00000245907.4:p.Glu1496Gln
|
|
ENST00000599668.1:n.81G>C
|
|
|
ENST00000599899.5:n.1445G>C
|
|
|
ENST00000601008.1:c.242-1509G>C
|
ENSP00000471384.1:n.242-1509G>C
|
|
NM_000064.3:c.4486G>C
|
NP_000055.2:p.Glu1496Gln
|
|
NM_000064.4:c.4486G>C
MANE Select
|
NP_000055.2:p.Glu1496Gln
|
|