|
NM_001378454.1:c.2059C>T
MANE Select
|
NP_001365383.1:p.His687Tyr
|
|
ENST00000613296.6:c.2059C>T
MANE Select
|
ENSP00000482968.1:p.His687Tyr
|
|
NM_015120.4:c.2062C>T , LRG_741t1:c.2062C>T
|
NP_055935.4:p.His688Tyr
|
|
ENST00000484298.5:c.1933C>T
|
ENSP00000478155.1:p.His645Tyr
|
|
ENST00000613296.4:c.2059C>T
|
ENSP00000482968.1:p.His687Tyr
|
|
ENST00000614410.4:c.2059C>T
|
ENSP00000479094.1:p.His687Tyr
|
|
ENST00000682565.1:c.1678C>T
|
ENSP00000507671.1:p.His560Tyr
|
|
ENST00000682801.1:c.1678C>T
|
ENSP00000507862.1:p.His560Tyr
|
|
ENST00000682859.1:c.1678C>T
|
ENSP00000508222.1:p.His560Tyr
|
|
ENST00000683791.1:c.685+16295C>T
|
|
|
ENST00000684548.1:c.1678C>T
|
ENSP00000507421.1:p.His560Tyr
|