ENST00000355943.8:c.1196A>G
MANE Select
|
ENSP00000348211.3:p.His399Arg
|
|
ENST00000355943.7:c.1196A>G
|
ENSP00000348211.3:p.His399Arg
|
|
ENST00000447245.6:c.953A>G
|
ENSP00000399717.2:p.His318Arg
|
|
ENST00000504098.1:c.758A>G
|
ENSP00000425708.1:p.His253Arg
|
|
ENST00000509432.1:c.557A>G
|
ENSP00000426604.1:p.His186Arg
|
|
ENST00000513706.2:n.2796A>G
|
|
|
ENST00000513807.5:c.710A>G
|
ENSP00000421134.1:p.His237Arg
|
|
NM_001303249.1:c.953A>G
|
NP_001290178.1:p.His318Arg
|
|
NM_001303250.1:c.923A>G
|
NP_001290179.1:p.His308Arg
|
|
NM_138773.2:c.1196A>G
|
NP_620128.1:p.His399Arg
|
|
NM_001303249.2:c.953A>G
|
NP_001290178.1:p.His318Arg
|
|
NM_001303250.2:c.923A>G
|
NP_001290179.1:p.His308Arg
|
|
NM_138773.3:c.1196A>G
|
NP_620128.1:p.His399Arg
|
|
NR_138151.1:n.1470A>G
|
|
|
NM_138773.4:c.1196A>G
MANE Select
|
NP_620128.1:p.His399Arg
|
|
NM_001303249.3:c.953A>G
|
NP_001290178.1:p.His318Arg
|
|
NM_001303250.3:c.923A>G
|
NP_001290179.1:p.His308Arg
|
|
NR_138151.2:n.1435A>G
|
|
|