ENST00000644719.2:c.651+27T>C
MANE Select
|
ENSP00000496625.1:n.651+27T>C
|
|
ENST00000418967.6:c.651+27T>C
|
ENSP00000408860.2:n.651+27T>C
|
|
ENST00000435122.3:c.561+27T>C
|
ENSP00000415043.2:n.561+27T>C
|
|
ENST00000462278.1:n.266T>C
|
|
|
ENST00000464325.5:n.572+27T>C
|
|
|
ENST00000466779.5:c.*343+27T>C
|
ENSP00000417321.1:n.*343+27T>C
|
|
ENST00000466879.5:n.702+27T>C
|
|
|
ENST00000479074.5:n.709+27T>C
|
|
|
ENST00000479730.5:n.767+27T>C
|
|
|
ENST00000483041.5:n.820+27T>C
|
|
|
ENST00000486063.5:n.831+27T>C
|
|
|
NM_000500.7:c.651+27T>C
|
NP_000491.4:n.651+27T>C
|
|
NM_001128590.3:c.561+27T>C
|
NP_001122062.3:n.561+27T>C
|
|
XM_011514314.1:c.246+27T>C
|
XP_011512616.1:n.246+27T>C
|
|
NM_000500.9:c.651+27T>C
MANE Select
|
NP_000491.4:n.651+27T>C
|
|
NM_001368143.1:c.246+27T>C
|
NP_001355072.1:n.246+27T>C
|
|
NM_001368144.1:c.246+27T>C
|
NP_001355073.1:n.246+27T>C
|
|
NM_001128590.4:c.561+27T>C
|
NP_001122062.3:n.561+27T>C
|
|
NM_001368143.2:c.246+27T>C
|
NP_001355072.1:n.246+27T>C
|
|
NM_001368144.2:c.246+27T>C
|
NP_001355073.1:n.246+27T>C
|
|