|
NM_001378454.1:c.5025C>G
MANE Select
|
NP_001365383.1:p.Tyr1675Ter
|
|
ENST00000613296.6:c.5025C>G
MANE Select
|
ENSP00000482968.1:p.Tyr1675Ter
|
|
NM_015120.4:c.5028C>G , LRG_741t1:c.5028C>G
|
NP_055935.4:p.Tyr1676Ter
|
|
ENST00000484298.5:c.4899C>G
|
ENSP00000478155.1:p.Tyr1633Ter
|
|
ENST00000613296.4:c.5025C>G
|
ENSP00000482968.1:p.Tyr1675Ter
|
|
ENST00000614410.4:c.5025C>G
|
ENSP00000479094.1:p.Tyr1675Ter
|
|
ENST00000682565.1:c.4644C>G
|
ENSP00000507671.1:p.Tyr1548Ter
|
|
ENST00000682801.1:c.4644C>G
|
ENSP00000507862.1:p.Tyr1548Ter
|
|
ENST00000682859.1:c.4644C>G
|
ENSP00000508222.1:p.Tyr1548Ter
|
|
ENST00000683791.1:c.685+19261C>G
|
|
|
ENST00000684460.1:c.2096C>G
|
|
|
ENST00000684548.1:c.4644C>G
|
ENSP00000507421.1:p.Tyr1548Ter
|
|
ENST00000684656.1:c.2096C>G
|
|