ENST00000355943.8:c.1139A>C
MANE Select
|
ENSP00000348211.3:p.Glu380Ala
|
|
ENST00000355943.7:c.1139A>C
|
ENSP00000348211.3:p.Glu380Ala
|
|
ENST00000447245.6:c.896A>C
|
ENSP00000399717.2:p.Glu299Ala
|
|
ENST00000504098.1:c.701A>C
|
ENSP00000425708.1:p.Glu234Ala
|
|
ENST00000509432.1:c.500A>C
|
ENSP00000426604.1:p.Glu167Ala
|
|
ENST00000513706.2:n.2739A>C
|
|
|
ENST00000513807.5:c.653A>C
|
ENSP00000421134.1:p.Glu218Ala
|
|
NM_001303249.1:c.896A>C
|
NP_001290178.1:p.Glu299Ala
|
|
NM_001303250.1:c.866A>C
|
NP_001290179.1:p.Glu289Ala
|
|
NM_138773.2:c.1139A>C
|
NP_620128.1:p.Glu380Ala
|
|
NM_001303249.2:c.896A>C
|
NP_001290178.1:p.Glu299Ala
|
|
NM_001303250.2:c.866A>C
|
NP_001290179.1:p.Glu289Ala
|
|
NM_138773.3:c.1139A>C
|
NP_620128.1:p.Glu380Ala
|
|
NR_138151.1:n.1413A>C
|
|
|
NM_138773.4:c.1139A>C
MANE Select
|
NP_620128.1:p.Glu380Ala
|
|
NM_001303249.3:c.896A>C
|
NP_001290178.1:p.Glu299Ala
|
|
NM_001303250.3:c.866A>C
|
NP_001290179.1:p.Glu289Ala
|
|
NR_138151.2:n.1378A>C
|
|
|