ENST00000355943.8:c.1245A>C
MANE Select
|
ENSP00000348211.3:p.Gln415His
|
|
ENST00000355943.7:c.1245A>C
|
ENSP00000348211.3:p.Gln415His
|
|
ENST00000447245.6:c.1002A>C
|
ENSP00000399717.2:p.Gln334His
|
|
ENST00000504098.1:c.807A>C
|
ENSP00000425708.1:p.Gln269His
|
|
ENST00000509432.1:c.606A>C
|
ENSP00000426604.1:p.Gln202His
|
|
ENST00000513706.2:n.2845A>C
|
|
|
ENST00000513807.5:c.759A>C
|
ENSP00000421134.1:p.Gln253His
|
|
NM_001303249.1:c.1002A>C
|
NP_001290178.1:p.Gln334His
|
|
NM_001303250.1:c.972A>C
|
NP_001290179.1:p.Gln324His
|
|
NM_138773.2:c.1245A>C
|
NP_620128.1:p.Gln415His
|
|
NM_001303249.2:c.1002A>C
|
NP_001290178.1:p.Gln334His
|
|
NM_001303250.2:c.972A>C
|
NP_001290179.1:p.Gln324His
|
|
NM_138773.3:c.1245A>C
|
NP_620128.1:p.Gln415His
|
|
NR_138151.1:n.1519A>C
|
|
|
NM_138773.4:c.1245A>C
MANE Select
|
NP_620128.1:p.Gln415His
|
|
NM_001303249.3:c.1002A>C
|
NP_001290178.1:p.Gln334His
|
|
NM_001303250.3:c.972A>C
|
NP_001290179.1:p.Gln324His
|
|
NR_138151.2:n.1484A>C
|
|
|