ENST00000272602.7:c.726T>C
MANE Select
|
ENSP00000272602.2:p.His242=
|
|
ENST00000272602.6:c.726T>C
|
ENSP00000272602.2:p.His242=
|
|
ENST00000393504.5:c.726T>C
|
ENSP00000377140.1:p.His242=
|
|
ENST00000409937.1:c.738T>C
|
ENSP00000386761.1:p.His246=
|
|
ENST00000436404.6:c.672T>C
|
ENSP00000410070.2:p.His224=
|
|
NM_001079878.1:c.672T>C
|
NP_001073347.1:p.His224=
|
|
NM_001298.2:c.726T>C
|
NP_001289.1:p.His242=
|
|
XM_006712243.2:c.837T>C
|
XP_006712306.1:p.His279=
|
|
XM_011510554.1:c.891T>C
|
XP_011508856.1:p.His297=
|
|
XM_011510554.2:c.891T>C
|
XP_011508856.1:p.His297=
|
|
NM_001079878.2:c.672T>C
|
NP_001073347.1:p.His224=
|
|
NM_001298.3:c.726T>C
MANE Select
|
NP_001289.1:p.His242=
|
|