ENST00000355943.8:c.1245A>G
MANE Select
|
ENSP00000348211.3:p.Gln415=
|
|
ENST00000355943.7:c.1245A>G
|
ENSP00000348211.3:p.Gln415=
|
|
ENST00000447245.6:c.1002A>G
|
ENSP00000399717.2:p.Gln334=
|
|
ENST00000504098.1:c.807A>G
|
ENSP00000425708.1:p.Gln269=
|
|
ENST00000509432.1:c.606A>G
|
ENSP00000426604.1:p.Gln202=
|
|
ENST00000513706.2:n.2845A>G
|
|
|
ENST00000513807.5:c.759A>G
|
ENSP00000421134.1:p.Gln253=
|
|
NM_001303249.1:c.1002A>G
|
NP_001290178.1:p.Gln334=
|
|
NM_001303250.1:c.972A>G
|
NP_001290179.1:p.Gln324=
|
|
NM_138773.2:c.1245A>G
|
NP_620128.1:p.Gln415=
|
|
NM_001303249.2:c.1002A>G
|
NP_001290178.1:p.Gln334=
|
|
NM_001303250.2:c.972A>G
|
NP_001290179.1:p.Gln324=
|
|
NM_138773.3:c.1245A>G
|
NP_620128.1:p.Gln415=
|
|
NR_138151.1:n.1519A>G
|
|
|
NM_138773.4:c.1245A>G
MANE Select
|
NP_620128.1:p.Gln415=
|
|
NM_001303249.3:c.1002A>G
|
NP_001290178.1:p.Gln334=
|
|
NM_001303250.3:c.972A>G
|
NP_001290179.1:p.Gln324=
|
|
NR_138151.2:n.1484A>G
|
|
|