ENST00000695651.1:n.2689C>G
|
|
|
ENST00000695653.1:c.2250C>G
|
ENSP00000512084.1:p.Tyr750Ter
|
|
ENST00000695654.1:c.3366C>G
|
ENSP00000512085.1:p.Tyr1122Ter
|
|
ENST00000695689.1:c.312C>G
|
ENSP00000512101.1:n.312C>G
|
|
ENST00000695690.1:n.532C>G
|
|
|
ENST00000695691.1:n.532C>G
|
|
|
ENST00000245907.11:c.4341C>G
MANE Select
|
ENSP00000245907.4:p.Tyr1447Ter
|
|
ENST00000245907.10:c.4341C>G
|
ENSP00000245907.4:p.Tyr1447Ter
|
|
ENST00000596548.1:c.462C>G
|
ENSP00000469744.1:p.Tyr154Ter
|
|
ENST00000599899.5:n.1300C>G
|
|
|
ENST00000601008.1:c.242-3992C>G
|
ENSP00000471384.1:n.242-3992C>G
|
|
NM_000064.3:c.4341C>G
|
NP_000055.2:p.Tyr1447Ter
|
|
NM_000064.4:c.4341C>G
MANE Select
|
NP_000055.2:p.Tyr1447Ter
|
|