ENST00000644719.2:c.727A>T
MANE Select
|
ENSP00000496625.1:p.Arg243Trp
|
|
ENST00000418967.6:c.727A>T
|
ENSP00000408860.2:p.Arg243Trp
|
|
ENST00000435122.3:c.637A>T
|
ENSP00000415043.2:p.Arg213Trp
|
|
ENST00000462278.1:n.416A>T
|
|
|
ENST00000466779.5:c.*419A>T
|
ENSP00000417321.1:n.*419A>T
|
|
ENST00000479074.5:n.785A>T
|
|
|
ENST00000479730.5:n.843A>T
|
|
|
ENST00000483041.5:n.896A>T
|
|
|
ENST00000486063.5:n.907A>T
|
|
|
NM_000500.7:c.727A>T
|
NP_000491.4:p.Arg243Trp
|
|
NM_001128590.3:c.637A>T
|
NP_001122062.3:p.Arg213Trp
|
|
XM_011514314.1:c.322A>T
|
XP_011512616.1:p.Arg108Trp
|
|
NM_000500.9:c.727A>T
MANE Select
|
NP_000491.4:p.Arg243Trp
|
|
NM_001368143.1:c.322A>T
|
NP_001355072.1:p.Arg108Trp
|
|
NM_001368144.1:c.322A>T
|
NP_001355073.1:p.Arg108Trp
|
|
NM_001128590.4:c.637A>T
|
NP_001122062.3:p.Arg213Trp
|
|
NM_001368143.2:c.322A>T
|
NP_001355072.1:p.Arg108Trp
|
|
NM_001368144.2:c.322A>T
|
NP_001355073.1:p.Arg108Trp
|
|