ENST00000355943.8:c.1257A>C
MANE Select
|
ENSP00000348211.3:p.Ter419Cys
|
|
ENST00000355943.7:c.1257A>C
|
ENSP00000348211.3:p.Ter419Cys
|
|
ENST00000447245.6:c.1014A>C
|
ENSP00000399717.2:p.Ter338Cys
|
|
ENST00000504098.1:c.819A>C
|
ENSP00000425708.1:p.Ter273Cys
|
|
ENST00000509432.1:c.618A>C
|
ENSP00000426604.1:p.Ter206Cys
|
|
ENST00000513706.2:n.2857A>C
|
|
|
ENST00000513807.5:c.771A>C
|
ENSP00000421134.1:p.Ter257Cys
|
|
NM_001303249.1:c.1014A>C
|
NP_001290178.1:p.Ter338Cys
|
|
NM_001303250.1:c.984A>C
|
NP_001290179.1:p.Ter328Cys
|
|
NM_138773.2:c.1257A>C
|
NP_620128.1:p.Ter419Cys
|
|
NM_001303249.2:c.1014A>C
|
NP_001290178.1:p.Ter338Cys
|
|
NM_001303250.2:c.984A>C
|
NP_001290179.1:p.Ter328Cys
|
|
NM_138773.3:c.1257A>C
|
NP_620128.1:p.Ter419Cys
|
|
NR_138151.1:n.1531A>C
|
|
|
NM_138773.4:c.1257A>C
MANE Select
|
NP_620128.1:p.Ter419Cys
|
|
NM_001303249.3:c.1014A>C
|
NP_001290178.1:p.Ter338Cys
|
|
NM_001303250.3:c.984A>C
|
NP_001290179.1:p.Ter328Cys
|
|
NR_138151.2:n.1496A>C
|
|
|