ENST00000644719.2:c.1213T>G
MANE Select
|
ENSP00000496625.1:p.Phe405Val
|
|
ENST00000418967.6:c.1213T>G
|
ENSP00000408860.2:p.Phe405Val
|
|
ENST00000435122.3:c.1123T>G
|
ENSP00000415043.2:p.Phe375Val
|
|
ENST00000479074.5:n.1354T>G
|
|
|
ENST00000479730.5:n.1329T>G
|
|
|
ENST00000483041.5:n.1382T>G
|
|
|
ENST00000486063.5:n.1192T>G
|
|
|
NM_000500.7:c.1213T>G
|
NP_000491.4:p.Phe405Val
|
|
NM_001128590.3:c.1123T>G
|
NP_001122062.3:p.Phe375Val
|
|
XM_011514314.1:c.808T>G
|
XP_011512616.1:p.Phe270Val
|
|
NM_000500.9:c.1213T>G
MANE Select
|
NP_000491.4:p.Phe405Val
|
|
NM_001368143.1:c.808T>G
|
NP_001355072.1:p.Phe270Val
|
|
NM_001368144.1:c.808T>G
|
NP_001355073.1:p.Phe270Val
|
|
NM_001128590.4:c.1123T>G
|
NP_001122062.3:p.Phe375Val
|
|
NM_001368143.2:c.808T>G
|
NP_001355072.1:p.Phe270Val
|
|
NM_001368144.2:c.808T>G
|
NP_001355073.1:p.Phe270Val
|
|