ENST00000644719.2:c.589G=
MANE Select
|
ENSP00000496625.1:p.Glu197=
|
|
ENST00000418967.6:c.589G=
|
ENSP00000408860.2:p.Glu197=
|
|
ENST00000435122.3:c.499G=
|
ENSP00000415043.2:p.Glu167=
|
|
ENST00000462278.1:n.177G=
|
|
|
ENST00000464325.5:n.510G=
|
|
|
ENST00000466779.5:c.*281G=
|
ENSP00000417321.1:n.*281G=
|
|
ENST00000466879.5:n.640G=
|
|
|
ENST00000469053.5:c.*281G=
|
ENSP00000418104.1:n.*281G=
|
|
ENST00000471671.4:c.550G=
|
ENSP00000418561.1:p.Glu184=
|
|
ENST00000479074.5:n.647G=
|
|
|
ENST00000479730.5:n.705G=
|
|
|
ENST00000483041.5:n.758G=
|
|
|
ENST00000486063.5:n.769G=
|
|
|
NM_000500.7:c.589G=
|
NP_000491.4:p.Glu197=
|
|
NM_001128590.3:c.499G=
|
NP_001122062.3:p.Glu167=
|
|
XM_011514314.1:c.184G=
|
XP_011512616.1:p.Glu62=
|
|
NM_000500.9:c.589G=
MANE Select
|
NP_000491.4:p.Glu197=
|
|
NM_001368143.1:c.184G=
|
NP_001355072.1:p.Glu62=
|
|
NM_001368144.1:c.184G=
|
NP_001355073.1:p.Glu62=
|
|
NM_001128590.4:c.499G=
|
NP_001122062.3:p.Glu167=
|
|
NM_001368143.2:c.184G=
|
NP_001355072.1:p.Glu62=
|
|
NM_001368144.2:c.184G=
|
NP_001355073.1:p.Glu62=
|
|