ENST00000644719.2:c.*13G>T
MANE Select
|
ENSP00000496625.1:n.*13G>T
|
|
ENST00000418967.6:c.*13G>T
|
ENSP00000408860.2:n.*13G>T
|
|
ENST00000435122.3:c.*13G>T
|
ENSP00000415043.2:n.*13G>T
|
|
ENST00000479074.5:n.1642G>T
|
|
|
ENST00000479730.5:n.1617G>T
|
|
|
ENST00000483041.5:n.1670G>T
|
|
|
ENST00000486063.5:n.1480G>T
|
|
|
NM_000500.7:c.*13G>T
|
NP_000491.4:n.*13G>T
|
|
NM_001128590.3:c.*13G>T
|
NP_001122062.3:n.*13G>T
|
|
XM_011514314.1:c.*13G>T
|
XP_011512616.1:n.*13G>T
|
|
NM_000500.9:c.*13G>T
MANE Select
|
NP_000491.4:n.*13G>T
|
|
NM_001368143.1:c.*13G>T
|
NP_001355072.1:n.*13G>T
|
|
NM_001368144.1:c.*13G>T
|
NP_001355073.1:n.*13G>T
|
|
NM_001128590.4:c.*13G>T
|
NP_001122062.3:n.*13G>T
|
|
NM_001368143.2:c.*13G>T
|
NP_001355072.1:n.*13G>T
|
|
NM_001368144.2:c.*13G>T
|
NP_001355073.1:n.*13G>T
|
|