ENST00000644719.2:c.1118G=
MANE Select
|
ENSP00000496625.1:p.Ser373=
|
|
ENST00000418967.6:c.1118G=
|
ENSP00000408860.2:p.Ser373=
|
|
ENST00000435122.3:c.1028G=
|
ENSP00000415043.2:p.Ser343=
|
|
ENST00000479074.5:n.1176G=
|
|
|
ENST00000479730.5:n.1234G=
|
|
|
ENST00000483041.5:n.1287G=
|
|
|
ENST00000486063.5:n.1097G=
|
|
|
NM_000500.7:c.1118G=
|
NP_000491.4:p.Ser373=
|
|
NM_001128590.3:c.1028G=
|
NP_001122062.3:p.Ser343=
|
|
XM_011514314.1:c.713G=
|
XP_011512616.1:p.Ser238=
|
|
NM_000500.9:c.1118G=
MANE Select
|
NP_000491.4:p.Ser373=
|
|
NM_001368143.1:c.713G=
|
NP_001355072.1:p.Ser238=
|
|
NM_001368144.1:c.713G=
|
NP_001355073.1:p.Ser238=
|
|
NM_001128590.4:c.1028G=
|
NP_001122062.3:p.Ser343=
|
|
NM_001368143.2:c.713G=
|
NP_001355072.1:p.Ser238=
|
|
NM_001368144.2:c.713G=
|
NP_001355073.1:p.Ser238=
|
|