ENST00000644719.2:c.618C>A
MANE Select
|
ENSP00000496625.1:p.Ser206=
|
|
ENST00000418967.6:c.618C>A
|
ENSP00000408860.2:p.Ser206=
|
|
ENST00000435122.3:c.528C>A
|
ENSP00000415043.2:p.Ser176=
|
|
ENST00000462278.1:n.206C>A
|
|
|
ENST00000464325.5:n.539C>A
|
|
|
ENST00000466779.5:c.*310C>A
|
ENSP00000417321.1:n.*310C>A
|
|
ENST00000466879.5:n.669C>A
|
|
|
ENST00000469053.5:c.*310C>A
|
ENSP00000418104.1:n.*310C>A
|
|
ENST00000479074.5:n.676C>A
|
|
|
ENST00000479730.5:n.734C>A
|
|
|
ENST00000483041.5:n.787C>A
|
|
|
ENST00000486063.5:n.798C>A
|
|
|
NM_000500.7:c.618C>A
|
NP_000491.4:p.Ser206=
|
|
NM_001128590.3:c.528C>A
|
NP_001122062.3:p.Ser176=
|
|
XM_011514314.1:c.213C>A
|
XP_011512616.1:p.Ser71=
|
|
NM_000500.9:c.618C>A
MANE Select
|
NP_000491.4:p.Ser206=
|
|
NM_001368143.1:c.213C>A
|
NP_001355072.1:p.Ser71=
|
|
NM_001368144.1:c.213C>A
|
NP_001355073.1:p.Ser71=
|
|
NM_001128590.4:c.528C>A
|
NP_001122062.3:p.Ser176=
|
|
NM_001368143.2:c.213C>A
|
NP_001355072.1:p.Ser71=
|
|
NM_001368144.2:c.213C>A
|
NP_001355073.1:p.Ser71=
|
|