ENST00000644719.2:c.739-41C>T
MANE Select
|
ENSP00000496625.1:n.739-41C>T
|
|
ENST00000418967.6:c.739-41C>T
|
ENSP00000408860.2:n.739-41C>T
|
|
ENST00000435122.3:c.649-41C>T
|
ENSP00000415043.2:n.649-41C>T
|
|
ENST00000462278.1:n.556C>T
|
|
|
ENST00000479074.5:n.797-41C>T
|
|
|
ENST00000479730.5:n.855-41C>T
|
|
|
ENST00000483041.5:n.908-41C>T
|
|
|
ENST00000486063.5:n.918+129C>T
|
|
|
NM_000500.7:c.739-41C>T
|
NP_000491.4:n.739-41C>T
|
|
NM_001128590.3:c.649-41C>T
|
NP_001122062.3:n.649-41C>T
|
|
XM_011514314.1:c.334-41C>T
|
XP_011512616.1:n.334-41C>T
|
|
NM_000500.9:c.739-41C>T
MANE Select
|
NP_000491.4:n.739-41C>T
|
|
NM_001368143.1:c.334-41C>T
|
NP_001355072.1:n.334-41C>T
|
|
NM_001368144.1:c.334-41C>T
|
NP_001355073.1:n.334-41C>T
|
|
NM_001128590.4:c.649-41C>T
|
NP_001122062.3:n.649-41C>T
|
|
NM_001368143.2:c.334-41C>T
|
NP_001355072.1:n.334-41C>T
|
|
NM_001368144.2:c.334-41C>T
|
NP_001355073.1:n.334-41C>T
|
|