ENST00000355943.8:c.1191A>G
MANE Select
|
ENSP00000348211.3:p.Thr397=
|
|
ENST00000355943.7:c.1191A>G
|
ENSP00000348211.3:p.Thr397=
|
|
ENST00000447245.6:c.948A>G
|
ENSP00000399717.2:p.Thr316=
|
|
ENST00000504098.1:c.753A>G
|
ENSP00000425708.1:p.Thr251=
|
|
ENST00000509432.1:c.552A>G
|
ENSP00000426604.1:p.Thr184=
|
|
ENST00000513706.2:n.2791A>G
|
|
|
ENST00000513807.5:c.705A>G
|
ENSP00000421134.1:p.Thr235=
|
|
NM_001303249.1:c.948A>G
|
NP_001290178.1:p.Thr316=
|
|
NM_001303250.1:c.918A>G
|
NP_001290179.1:p.Thr306=
|
|
NM_138773.2:c.1191A>G
|
NP_620128.1:p.Thr397=
|
|
NM_001303249.2:c.948A>G
|
NP_001290178.1:p.Thr316=
|
|
NM_001303250.2:c.918A>G
|
NP_001290179.1:p.Thr306=
|
|
NM_138773.3:c.1191A>G
|
NP_620128.1:p.Thr397=
|
|
NR_138151.1:n.1465A>G
|
|
|
NM_138773.4:c.1191A>G
MANE Select
|
NP_620128.1:p.Thr397=
|
|
NM_001303249.3:c.948A>G
|
NP_001290178.1:p.Thr316=
|
|
NM_001303250.3:c.918A>G
|
NP_001290179.1:p.Thr306=
|
|
NR_138151.2:n.1430A>G
|
|
|