ENST00000682565.1:c.10183C>T
|
ENSP00000507671.1:p.His3395Tyr
|
|
ENST00000682801.1:c.10183C>T
|
ENSP00000507862.1:p.His3395Tyr
|
|
ENST00000682859.1:c.10183C>T
|
ENSP00000508222.1:p.His3395Tyr
|
|
ENST00000683791.1:c.3269C>T
|
|
|
ENST00000684460.1:c.7464C>T
|
|
|
ENST00000684548.1:c.10183C>T
|
ENSP00000507421.1:p.His3395Tyr
|
|
ENST00000684590.1:c.4630C>T
|
ENSP00000507376.1:p.His1544Tyr
|
|
ENST00000684656.1:c.7509C>T
|
|
|
ENST00000613296.6:c.10564C>T
MANE Select
|
ENSP00000482968.1:p.His3522Tyr
|
|
ENST00000651057.1:c.718C>T
|
ENSP00000498504.1:p.His240Tyr
|
|
ENST00000651434.1:c.1920C>T
|
|
|
ENST00000652487.1:c.1661C>T
|
|
|
ENST00000423048.5:c.4055C>T
|
ENSP00000399833.1:n.4055C>T
|
|
ENST00000484298.5:c.10438C>T
|
ENSP00000478155.1:p.His3480Tyr
|
|
ENST00000613296.4:c.10564C>T
|
ENSP00000482968.1:p.His3522Tyr
|
|
ENST00000614410.4:c.10564C>T
|
ENSP00000479094.1:p.His3522Tyr
|
|
ENST00000620466.4:n.4367C>T
|
|
|
NM_015120.4:c.10567C>T , LRG_741t1:c.10567C>T
|
NP_055935.4:p.His3523Tyr
|
|
NM_001378454.1:c.10564C>T
MANE Select
|
NP_001365383.1:p.His3522Tyr
|
|