ENST00000644719.2:c.1003G>T
MANE Select
|
ENSP00000496625.1:p.Val335Phe
|
|
ENST00000418967.6:c.1003G>T
|
ENSP00000408860.2:p.Val335Phe
|
|
ENST00000435122.3:c.913G>T
|
ENSP00000415043.2:p.Val305Phe
|
|
ENST00000479074.5:n.1061G>T
|
|
|
ENST00000479730.5:n.1119G>T
|
|
|
ENST00000483041.5:n.1172G>T
|
|
|
ENST00000486063.5:n.982G>T
|
|
|
NM_000500.7:c.1003G>T
|
NP_000491.4:p.Val335Phe
|
|
NM_001128590.3:c.913G>T
|
NP_001122062.3:p.Val305Phe
|
|
XM_011514314.1:c.598G>T
|
XP_011512616.1:p.Val200Phe
|
|
NM_000500.9:c.1003G>T
MANE Select
|
NP_000491.4:p.Val335Phe
|
|
NM_001368143.1:c.598G>T
|
NP_001355072.1:p.Val200Phe
|
|
NM_001368144.1:c.598G>T
|
NP_001355073.1:p.Val200Phe
|
|
NM_001128590.4:c.913G>T
|
NP_001122062.3:p.Val305Phe
|
|
NM_001368143.2:c.598G>T
|
NP_001355072.1:p.Val200Phe
|
|
NM_001368144.2:c.598G>T
|
NP_001355073.1:p.Val200Phe
|
|