ENST00000355943.8:c.1186T>C
MANE Select
|
ENSP00000348211.3:p.Tyr396His
|
|
ENST00000355943.7:c.1186T>C
|
ENSP00000348211.3:p.Tyr396His
|
|
ENST00000447245.6:c.943T>C
|
ENSP00000399717.2:p.Tyr315His
|
|
ENST00000504098.1:c.748T>C
|
ENSP00000425708.1:p.Tyr250His
|
|
ENST00000509432.1:c.547T>C
|
ENSP00000426604.1:p.Tyr183His
|
|
ENST00000513706.2:n.2786T>C
|
|
|
ENST00000513807.5:c.700T>C
|
ENSP00000421134.1:p.Tyr234His
|
|
NM_001303249.1:c.943T>C
|
NP_001290178.1:p.Tyr315His
|
|
NM_001303250.1:c.913T>C
|
NP_001290179.1:p.Tyr305His
|
|
NM_138773.2:c.1186T>C
|
NP_620128.1:p.Tyr396His
|
|
NM_001303249.2:c.943T>C
|
NP_001290178.1:p.Tyr315His
|
|
NM_001303250.2:c.913T>C
|
NP_001290179.1:p.Tyr305His
|
|
NM_138773.3:c.1186T>C
|
NP_620128.1:p.Tyr396His
|
|
NR_138151.1:n.1460T>C
|
|
|
NM_138773.4:c.1186T>C
MANE Select
|
NP_620128.1:p.Tyr396His
|
|
NM_001303249.3:c.943T>C
|
NP_001290178.1:p.Tyr315His
|
|
NM_001303250.3:c.913T>C
|
NP_001290179.1:p.Tyr305His
|
|
NR_138151.2:n.1425T>C
|
|
|