ENST00000644719.2:c.1222G>C
MANE Select
|
ENSP00000496625.1:p.Asp408His
|
|
ENST00000418967.6:c.1222G>C
|
ENSP00000408860.2:p.Asp408His
|
|
ENST00000435122.3:c.1132G>C
|
ENSP00000415043.2:p.Asp378His
|
|
ENST00000479074.5:n.1363G>C
|
|
|
ENST00000479730.5:n.1338G>C
|
|
|
ENST00000483041.5:n.1391G>C
|
|
|
ENST00000486063.5:n.1201G>C
|
|
|
NM_000500.7:c.1222G>C
|
NP_000491.4:p.Asp408His
|
|
NM_001128590.3:c.1132G>C
|
NP_001122062.3:p.Asp378His
|
|
XM_011514314.1:c.817G>C
|
XP_011512616.1:p.Asp273His
|
|
NM_000500.9:c.1222G>C
MANE Select
|
NP_000491.4:p.Asp408His
|
|
NM_001368143.1:c.817G>C
|
NP_001355072.1:p.Asp273His
|
|
NM_001368144.1:c.817G>C
|
NP_001355073.1:p.Asp273His
|
|
NM_001128590.4:c.1132G>C
|
NP_001122062.3:p.Asp378His
|
|
NM_001368143.2:c.817G>C
|
NP_001355072.1:p.Asp273His
|
|
NM_001368144.2:c.817G>C
|
NP_001355073.1:p.Asp273His
|
|