ENST00000644719.2:c.292+126G>T
MANE Select
|
ENSP00000496625.1:n.292+126G>T
|
|
ENST00000418967.6:c.292+126G>T
|
ENSP00000408860.2:n.292+126G>T
|
|
ENST00000435122.3:c.203-157G>T
|
ENSP00000415043.2:n.203-157G>T
|
|
ENST00000464325.5:n.229+126G>T
|
|
|
ENST00000466779.5:c.292+126G>T
|
ENSP00000417321.1:n.292+126G>T
|
|
ENST00000466879.5:n.187G>T
|
|
|
ENST00000469053.5:c.203-138G>T
|
ENSP00000418104.1:n.203-138G>T
|
|
ENST00000471671.4:c.292+126G>T
|
ENSP00000418561.1:n.292+126G>T
|
|
ENST00000478281.5:c.293-124G>T
|
ENSP00000419572.1:n.293-124G>T
|
|
ENST00000479074.5:n.350+126G>T
|
|
|
ENST00000479730.5:n.447+126G>T
|
|
|
ENST00000480027.1:n.471G>T
|
|
|
ENST00000483041.5:n.442+126G>T
|
|
|
ENST00000486063.5:n.472+126G>T
|
|
|
ENST00000488465.1:n.300+126G>T
|
|
|
NM_000500.7:c.292+126G>T
|
NP_000491.4:n.292+126G>T
|
|
NM_001128590.3:c.203-157G>T
|
NP_001122062.3:n.203-157G>T
|
|
XM_011514314.1:c.-133+126G>T
|
XP_011512616.1:n.-133+126G>T
|
|
NM_000500.9:c.292+126G>T
MANE Select
|
NP_000491.4:n.292+126G>T
|
|
NM_001368143.1:c.-133+126G>T
|
NP_001355072.1:n.-133+126G>T
|
|
NM_001368144.1:c.-132-138G>T
|
NP_001355073.1:n.-132-138G>T
|
|
NM_001128590.4:c.203-157G>T
|
NP_001122062.3:n.203-157G>T
|
|
NM_001368143.2:c.-133+126G>T
|
NP_001355072.1:n.-133+126G>T
|
|
NM_001368144.2:c.-132-138G>T
|
NP_001355073.1:n.-132-138G>T
|
|