ENST00000644719.2:c.483T>A
MANE Select
|
ENSP00000496625.1:p.Ile161=
|
|
ENST00000418967.6:c.483T>A
|
ENSP00000408860.2:p.Ile161=
|
|
ENST00000435122.3:c.393T>A
|
ENSP00000415043.2:p.Ile131=
|
|
ENST00000462278.1:n.71T>A
|
|
|
ENST00000464325.5:n.404T>A
|
|
|
ENST00000466779.5:c.*175T>A
|
ENSP00000417321.1:n.*175T>A
|
|
ENST00000466879.5:n.534T>A
|
|
|
ENST00000469053.5:c.*175T>A
|
ENSP00000418104.1:n.*175T>A
|
|
ENST00000471671.4:c.483T>A
|
ENSP00000418561.1:p.Ile161=
|
|
ENST00000478281.5:c.516T>A
|
ENSP00000419572.1:p.Ile172=
|
|
ENST00000479074.5:n.541T>A
|
|
|
ENST00000479730.5:n.638T>A
|
|
|
ENST00000483041.5:n.652T>A
|
|
|
ENST00000486063.5:n.663T>A
|
|
|
ENST00000488465.1:n.491T>A
|
|
|
NM_000500.7:c.483T>A
|
NP_000491.4:p.Ile161=
|
|
NM_001128590.3:c.393T>A
|
NP_001122062.3:p.Ile131=
|
|
XM_011514314.1:c.78T>A
|
XP_011512616.1:p.Ile26=
|
|
NM_000500.9:c.483T>A
MANE Select
|
NP_000491.4:p.Ile161=
|
|
NM_001368143.1:c.78T>A
|
NP_001355072.1:p.Ile26=
|
|
NM_001368144.1:c.78T>A
|
NP_001355073.1:p.Ile26=
|
|
NM_001128590.4:c.393T>A
|
NP_001122062.3:p.Ile131=
|
|
NM_001368143.2:c.78T>A
|
NP_001355072.1:p.Ile26=
|
|
NM_001368144.2:c.78T>A
|
NP_001355073.1:p.Ile26=
|
|