ENST00000695651.1:n.2835A>G
|
|
|
ENST00000695653.1:c.2396A>G
|
ENSP00000512084.1:p.Glu799Gly
|
|
ENST00000695654.1:c.3512A>G
|
ENSP00000512085.1:p.Glu1171Gly
|
|
ENST00000695689.1:c.458A>G
|
ENSP00000512101.1:n.458A>G
|
|
ENST00000695690.1:n.1552A>G
|
|
|
ENST00000695691.1:n.1348A>G
|
|
|
ENST00000245907.11:c.4487A>G
MANE Select
|
ENSP00000245907.4:p.Glu1496Gly
|
|
ENST00000245907.10:c.4487A>G
|
ENSP00000245907.4:p.Glu1496Gly
|
|
ENST00000599668.1:n.82A>G
|
|
|
ENST00000599899.5:n.1446A>G
|
|
|
ENST00000601008.1:c.242-1508A>G
|
ENSP00000471384.1:n.242-1508A>G
|
|
NM_000064.3:c.4487A>G
|
NP_000055.2:p.Glu1496Gly
|
|
NM_000064.4:c.4487A>G
MANE Select
|
NP_000055.2:p.Glu1496Gly
|
|