ENST00000682587.1:c.246T>C
|
ENSP00000507403.1:p.His82=
|
|
ENST00000418600.7:c.504T>C
|
ENSP00000403636.3:p.His168=
|
|
ENST00000449372.7:c.504T>C
|
ENSP00000416519.4:p.His168=
|
|
ENST00000629380.3:c.504T>C
|
ENSP00000486463.1:p.His168=
|
|
ENST00000638142.2:c.504T>C
|
ENSP00000490803.1:p.His168=
|
|
ENST00000644458.1:c.504T>C
|
ENSP00000495541.1:p.His168=
|
|
ENST00000645250.1:c.327T>C
|
ENSP00000494861.1:p.His109=
|
|
ENST00000646630.1:c.504T>C
MANE Select
|
ENSP00000496007.1:p.His168=
|
|
ENST00000293748.9:c.459T>C
|
ENSP00000293748.6:p.His153=
|
|
ENST00000418600.6:c.504T>C
|
ENSP00000403636.3:p.His168=
|
|
ENST00000428982.4:c.327T>C
|
ENSP00000412475.2:p.His109=
|
|
ENST00000449372.6:c.504T>C
|
ENSP00000416519.3:p.His168=
|
|
ENST00000479510.2:n.699T>C
|
|
|
ENST00000628646.2:c.504T>C
|
ENSP00000486431.1:p.His168=
|
|
ENST00000629380.2:c.504T>C
|
ENSP00000486463.1:p.His168=
|
|
NM_006772.2:c.504T>C
|
NP_006763.2:p.His168=
|
|
NM_001130066.1:c.504T>C
|
NP_001123538.1:p.His168=
|
|
NM_001130066.2:c.504T>C
|
NP_001123538.1:p.His168=
|
|
NM_006772.3:c.504T>C
MANE Select
|
NP_006763.2:p.His168=
|
|