ENST00000355943.8:c.1222A>G
MANE Select
|
ENSP00000348211.3:p.Ile408Val
|
|
ENST00000355943.7:c.1222A>G
|
ENSP00000348211.3:p.Ile408Val
|
|
ENST00000447245.6:c.979A>G
|
ENSP00000399717.2:p.Ile327Val
|
|
ENST00000504098.1:c.784A>G
|
ENSP00000425708.1:p.Ile262Val
|
|
ENST00000509432.1:c.583A>G
|
ENSP00000426604.1:p.Ile195Val
|
|
ENST00000513706.2:n.2822A>G
|
|
|
ENST00000513807.5:c.736A>G
|
ENSP00000421134.1:p.Ile246Val
|
|
NM_001303249.1:c.979A>G
|
NP_001290178.1:p.Ile327Val
|
|
NM_001303250.1:c.949A>G
|
NP_001290179.1:p.Ile317Val
|
|
NM_138773.2:c.1222A>G
|
NP_620128.1:p.Ile408Val
|
|
NM_001303249.2:c.979A>G
|
NP_001290178.1:p.Ile327Val
|
|
NM_001303250.2:c.949A>G
|
NP_001290179.1:p.Ile317Val
|
|
NM_138773.3:c.1222A>G
|
NP_620128.1:p.Ile408Val
|
|
NR_138151.1:n.1496A>G
|
|
|
NM_138773.4:c.1222A>G
MANE Select
|
NP_620128.1:p.Ile408Val
|
|
NM_001303249.3:c.979A>G
|
NP_001290178.1:p.Ile327Val
|
|
NM_001303250.3:c.949A>G
|
NP_001290179.1:p.Ile317Val
|
|
NR_138151.2:n.1461A>G
|
|
|