ENST00000355943.8:c.1175T=
MANE Select
|
ENSP00000348211.3:p.Val392=
|
|
ENST00000355943.7:c.1175T=
|
ENSP00000348211.3:p.Val392=
|
|
ENST00000447245.6:c.932T=
|
ENSP00000399717.2:p.Val311=
|
|
ENST00000504098.1:c.737T=
|
ENSP00000425708.1:p.Val246=
|
|
ENST00000509432.1:c.536T=
|
ENSP00000426604.1:p.Val179=
|
|
ENST00000513706.2:n.2775T=
|
|
|
ENST00000513807.5:c.689T=
|
ENSP00000421134.1:p.Val230=
|
|
NM_001303249.1:c.932T=
|
NP_001290178.1:p.Val311=
|
|
NM_001303250.1:c.902T=
|
NP_001290179.1:p.Val301=
|
|
NM_138773.2:c.1175T=
|
NP_620128.1:p.Val392=
|
|
NM_001303249.2:c.932T=
|
NP_001290178.1:p.Val311=
|
|
NM_001303250.2:c.902T=
|
NP_001290179.1:p.Val301=
|
|
NM_138773.3:c.1175T=
|
NP_620128.1:p.Val392=
|
|
NR_138151.1:n.1449T=
|
|
|
NM_138773.4:c.1175T=
MANE Select
|
NP_620128.1:p.Val392=
|
|
NM_001303249.3:c.932T=
|
NP_001290178.1:p.Val311=
|
|
NM_001303250.3:c.902T=
|
NP_001290179.1:p.Val301=
|
|
NR_138151.2:n.1414T=
|
|
|