ENST00000644719.2:c.293-10C>G
MANE Select
|
ENSP00000496625.1:n.293-10C>G
|
|
ENST00000418967.6:c.293-10C>G
|
ENSP00000408860.2:n.293-10C>G
|
|
ENST00000435122.3:c.203-10C>G
|
ENSP00000415043.2:n.203-10C>G
|
|
ENST00000464325.5:n.230-26C>G
|
|
|
ENST00000466779.5:c.302C>G
|
ENSP00000417321.1:p.Ser101Cys
|
|
ENST00000466879.5:n.334C>G
|
|
|
ENST00000469053.5:c.212C>G
|
ENSP00000418104.1:p.Ser71Cys
|
|
ENST00000471671.4:c.293-10C>G
|
ENSP00000418561.1:n.293-10C>G
|
|
ENST00000478281.5:c.316C>G
|
ENSP00000419572.1:p.Pro106Ala
|
|
ENST00000479074.5:n.351-10C>G
|
|
|
ENST00000479730.5:n.448-10C>G
|
|
|
ENST00000480027.1:n.618C>G
|
|
|
ENST00000483041.5:n.452C>G
|
|
|
ENST00000486063.5:n.473-10C>G
|
|
|
ENST00000488465.1:n.301-10C>G
|
|
|
NM_000500.7:c.293-10C>G
|
NP_000491.4:n.293-10C>G
|
|
NM_001128590.3:c.203-10C>G
|
NP_001122062.3:n.203-10C>G
|
|
XM_011514314.1:c.-123C>G
|
XP_011512616.1:n.-123C>G
|
|
NM_000500.9:c.293-10C>G
MANE Select
|
NP_000491.4:n.293-10C>G
|
|
NM_001368143.1:c.-123C>G
|
NP_001355072.1:n.-123C>G
|
|
NM_001368144.1:c.-123C>G
|
NP_001355073.1:n.-123C>G
|
|
NM_001128590.4:c.203-10C>G
|
NP_001122062.3:n.203-10C>G
|
|
NM_001368143.2:c.-123C>G
|
NP_001355072.1:n.-123C>G
|
|
NM_001368144.2:c.-123C>G
|
NP_001355073.1:n.-123C>G
|
|