ENST00000355943.8:c.1179A>G
MANE Select
|
ENSP00000348211.3:p.Ile393Met
|
|
ENST00000355943.7:c.1179A>G
|
ENSP00000348211.3:p.Ile393Met
|
|
ENST00000447245.6:c.936A>G
|
ENSP00000399717.2:p.Ile312Met
|
|
ENST00000504098.1:c.741A>G
|
ENSP00000425708.1:p.Ile247Met
|
|
ENST00000509432.1:c.540A>G
|
ENSP00000426604.1:p.Ile180Met
|
|
ENST00000513706.2:n.2779A>G
|
|
|
ENST00000513807.5:c.693A>G
|
ENSP00000421134.1:p.Ile231Met
|
|
NM_001303249.1:c.936A>G
|
NP_001290178.1:p.Ile312Met
|
|
NM_001303250.1:c.906A>G
|
NP_001290179.1:p.Ile302Met
|
|
NM_138773.2:c.1179A>G
|
NP_620128.1:p.Ile393Met
|
|
NM_001303249.2:c.936A>G
|
NP_001290178.1:p.Ile312Met
|
|
NM_001303250.2:c.906A>G
|
NP_001290179.1:p.Ile302Met
|
|
NM_138773.3:c.1179A>G
|
NP_620128.1:p.Ile393Met
|
|
NR_138151.1:n.1453A>G
|
|
|
NM_138773.4:c.1179A>G
MANE Select
|
NP_620128.1:p.Ile393Met
|
|
NM_001303249.3:c.936A>G
|
NP_001290178.1:p.Ile312Met
|
|
NM_001303250.3:c.906A>G
|
NP_001290179.1:p.Ile302Met
|
|
NR_138151.2:n.1418A>G
|
|
|