ENST00000355943.8:c.1177A>G
MANE Select
|
ENSP00000348211.3:p.Ile393Val
|
|
ENST00000355943.7:c.1177A>G
|
ENSP00000348211.3:p.Ile393Val
|
|
ENST00000447245.6:c.934A>G
|
ENSP00000399717.2:p.Ile312Val
|
|
ENST00000504098.1:c.739A>G
|
ENSP00000425708.1:p.Ile247Val
|
|
ENST00000509432.1:c.538A>G
|
ENSP00000426604.1:p.Ile180Val
|
|
ENST00000513706.2:n.2777A>G
|
|
|
ENST00000513807.5:c.691A>G
|
ENSP00000421134.1:p.Ile231Val
|
|
NM_001303249.1:c.934A>G
|
NP_001290178.1:p.Ile312Val
|
|
NM_001303250.1:c.904A>G
|
NP_001290179.1:p.Ile302Val
|
|
NM_138773.2:c.1177A>G
|
NP_620128.1:p.Ile393Val
|
|
NM_001303249.2:c.934A>G
|
NP_001290178.1:p.Ile312Val
|
|
NM_001303250.2:c.904A>G
|
NP_001290179.1:p.Ile302Val
|
|
NM_138773.3:c.1177A>G
|
NP_620128.1:p.Ile393Val
|
|
NR_138151.1:n.1451A>G
|
|
|
NM_138773.4:c.1177A>G
MANE Select
|
NP_620128.1:p.Ile393Val
|
|
NM_001303249.3:c.934A>G
|
NP_001290178.1:p.Ile312Val
|
|
NM_001303250.3:c.904A>G
|
NP_001290179.1:p.Ile302Val
|
|
NR_138151.2:n.1416A>G
|
|
|