ENST00000644719.2:c.448-41G=
MANE Select
|
ENSP00000496625.1:n.448-41G=
|
|
ENST00000418967.6:c.448-41G=
|
ENSP00000408860.2:n.448-41G=
|
|
ENST00000435122.3:c.358-41G=
|
ENSP00000415043.2:n.358-41G=
|
|
ENST00000462278.1:n.36-41G=
|
|
|
ENST00000464325.5:n.369-41G=
|
|
|
ENST00000466779.5:c.*140-41G=
|
ENSP00000417321.1:n.*140-41G=
|
|
ENST00000466879.5:n.499-41G=
|
|
|
ENST00000469053.5:c.*140-41G=
|
ENSP00000418104.1:n.*140-41G=
|
|
ENST00000471671.4:c.448-41G=
|
ENSP00000418561.1:n.448-41G=
|
|
ENST00000478281.5:c.481-41G=
|
ENSP00000419572.1:n.481-41G=
|
|
ENST00000479074.5:n.506-41G=
|
|
|
ENST00000479730.5:n.603-41G=
|
|
|
ENST00000483041.5:n.617-41G=
|
|
|
ENST00000486063.5:n.628-41G=
|
|
|
ENST00000488465.1:n.456-41G=
|
|
|
NM_000500.7:c.448-41G=
|
NP_000491.4:n.448-41G=
|
|
NM_001128590.3:c.358-41G=
|
NP_001122062.3:n.358-41G=
|
|
XM_011514314.1:c.43-41G=
|
XP_011512616.1:n.43-41G=
|
|
NM_000500.9:c.448-41G=
MANE Select
|
NP_000491.4:n.448-41G=
|
|
NM_001368143.1:c.43-41G=
|
NP_001355072.1:n.43-41G=
|
|
NM_001368144.1:c.43-41G=
|
NP_001355073.1:n.43-41G=
|
|
NM_001128590.4:c.358-41G=
|
NP_001122062.3:n.358-41G=
|
|
NM_001368143.2:c.43-41G=
|
NP_001355072.1:n.43-41G=
|
|
NM_001368144.2:c.43-41G=
|
NP_001355073.1:n.43-41G=
|
|