ENST00000682565.1:c.10086C=
|
ENSP00000507671.1:p.His3362=
|
|
ENST00000682801.1:c.10086C=
|
ENSP00000507862.1:p.His3362=
|
|
ENST00000682859.1:c.10086C=
|
ENSP00000508222.1:p.His3362=
|
|
ENST00000683791.1:c.3172C=
|
|
|
ENST00000684460.1:c.7367C=
|
|
|
ENST00000684548.1:c.10086C=
|
ENSP00000507421.1:p.His3362=
|
|
ENST00000684590.1:c.4533C=
|
ENSP00000507376.1:p.His1511=
|
|
ENST00000684656.1:c.7412C=
|
|
|
ENST00000613296.6:c.10467C=
MANE Select
|
ENSP00000482968.1:p.His3489=
|
|
ENST00000651057.1:c.621C=
|
ENSP00000498504.1:p.His207=
|
|
ENST00000651434.1:c.1823C=
|
|
|
ENST00000652487.1:c.1564C=
|
|
|
ENST00000423048.5:c.3958C=
|
ENSP00000399833.1:n.3958C=
|
|
ENST00000484298.5:c.10341C=
|
ENSP00000478155.1:p.His3447=
|
|
ENST00000613296.4:c.10467C=
|
ENSP00000482968.1:p.His3489=
|
|
ENST00000614410.4:c.10467C=
|
ENSP00000479094.1:p.His3489=
|
|
ENST00000620466.4:n.4270C=
|
|
|
NM_015120.4:c.10470C= , LRG_741t1:c.10470C=
|
NP_055935.4:p.His3490=
|
|
NM_001378454.1:c.10467C=
MANE Select
|
NP_001365383.1:p.His3489=
|
|