ENST00000644719.2:c.681G>T
MANE Select
|
ENSP00000496625.1:p.Leu227=
|
|
ENST00000418967.6:c.681G>T
|
ENSP00000408860.2:p.Leu227=
|
|
ENST00000435122.3:c.591G>T
|
ENSP00000415043.2:p.Leu197=
|
|
ENST00000462278.1:n.370G>T
|
|
|
ENST00000466779.5:c.*373G>T
|
ENSP00000417321.1:n.*373G>T
|
|
ENST00000466879.5:n.732G>T
|
|
|
ENST00000479074.5:n.739G>T
|
|
|
ENST00000479730.5:n.797G>T
|
|
|
ENST00000483041.5:n.850G>T
|
|
|
ENST00000486063.5:n.861G>T
|
|
|
NM_000500.7:c.681G>T
|
NP_000491.4:p.Leu227=
|
|
NM_001128590.3:c.591G>T
|
NP_001122062.3:p.Leu197=
|
|
XM_011514314.1:c.276G>T
|
XP_011512616.1:p.Leu92=
|
|
NM_000500.9:c.681G>T
MANE Select
|
NP_000491.4:p.Leu227=
|
|
NM_001368143.1:c.276G>T
|
NP_001355072.1:p.Leu92=
|
|
NM_001368144.1:c.276G>T
|
NP_001355073.1:p.Leu92=
|
|
NM_001128590.4:c.591G>T
|
NP_001122062.3:p.Leu197=
|
|
NM_001368143.2:c.276G>T
|
NP_001355072.1:p.Leu92=
|
|
NM_001368144.2:c.276G>T
|
NP_001355073.1:p.Leu92=
|
|