ENST00000682565.1:c.11667C>G
|
ENSP00000507671.1:p.Tyr3889Ter
|
|
ENST00000682801.1:c.11167-815C>G
|
ENSP00000507862.1:n.11167-815C>G
|
|
ENST00000682859.1:c.11667C>G
|
ENSP00000508222.1:p.Tyr3889Ter
|
|
ENST00000683791.1:c.4753C>G
|
|
|
ENST00000684460.1:c.8948C>G
|
|
|
ENST00000684548.1:c.11667C>G
|
ENSP00000507421.1:p.Tyr3889Ter
|
|
ENST00000684590.1:c.6114C>G
|
ENSP00000507376.1:p.Tyr2038Ter
|
|
ENST00000684656.1:c.9132C>G
|
|
|
ENST00000613296.6:c.12048C>G
MANE Select
|
ENSP00000482968.1:p.Tyr4016Ter
|
|
ENST00000651057.1:c.2202C>G
|
ENSP00000498504.1:p.Tyr734Ter
|
|
ENST00000651434.1:c.3404C>G
|
|
|
ENST00000651750.1:c.1260+489C>G
|
|
|
ENST00000652487.1:c.3219C>G
|
|
|
ENST00000464408.3:n.223C>G
|
|
|
ENST00000484298.5:c.11922C>G
|
ENSP00000478155.1:p.Tyr3974Ter
|
|
ENST00000613296.4:c.12048C>G
|
ENSP00000482968.1:p.Tyr4016Ter
|
|
ENST00000620466.4:n.5851C>G
|
|
|
NM_015120.4:c.12051C>G , LRG_741t1:c.12051C>G
|
NP_055935.4:p.Tyr4017Ter
|
|
NM_001378454.1:c.12048C>G
MANE Select
|
NP_001365383.1:p.Tyr4016Ter
|
|