ENST00000695651.1:n.2522T>G
|
|
|
ENST00000695653.1:c.2083T>G
|
ENSP00000512084.1:p.Tyr695Asp
|
|
ENST00000695654.1:c.3199T>G
|
ENSP00000512085.1:p.Tyr1067Asp
|
|
ENST00000695689.1:c.145T>G
|
ENSP00000512101.1:n.145T>G
|
|
ENST00000695690.1:n.365T>G
|
|
|
ENST00000695691.1:n.365T>G
|
|
|
ENST00000245907.11:c.4174T>G
MANE Select
|
ENSP00000245907.4:p.Tyr1392Asp
|
|
ENST00000245907.10:c.4174T>G
|
ENSP00000245907.4:p.Tyr1392Asp
|
|
ENST00000596548.1:c.295T>G
|
ENSP00000469744.1:p.Tyr99Asp
|
|
ENST00000599899.5:n.1133T>G
|
|
|
ENST00000601008.1:c.242-4270T>G
|
ENSP00000471384.1:n.242-4270T>G
|
|
NM_000064.3:c.4174T>G
|
NP_000055.2:p.Tyr1392Asp
|
|
NM_000064.4:c.4174T>G
MANE Select
|
NP_000055.2:p.Tyr1392Asp
|
|