ENST00000567697.2:n.4020T>G
|
|
|
ENST00000682393.1:c.*258-1433T>G
|
ENSP00000506774.1:n.*258-1433T>G
|
|
ENST00000683094.1:c.*262-1433T>G
|
ENSP00000508230.1:n.*262-1433T>G
|
|
ENST00000683274.1:c.*180-1433T>G
|
ENSP00000507262.1:n.*180-1433T>G
|
|
ENST00000683435.1:c.*748T>G
|
ENSP00000508092.1:n.*748T>G
|
|
ENST00000268261.9:c.*111T>G
MANE Select
|
ENSP00000268261.4:n.*111T>G
|
|
ENST00000268261.8:c.*111T>G
|
ENSP00000268261.4:n.*111T>G
|
|
ENST00000562025.1:n.386T>G
|
|
|
ENST00000562318.5:c.*574T>G
|
ENSP00000454395.1:n.*574T>G
|
|
ENST00000565221.5:c.*470T>G
|
ENSP00000457932.1:n.*470T>G
|
|
ENST00000566540.5:c.*474T>G
|
ENSP00000454284.1:n.*474T>G
|
|
ENST00000566604.5:c.*392T>G
|
ENSP00000456774.1:n.*392T>G
|
|
ENST00000567697.1:n.4020T>G
|
|
|
ENST00000569958.5:c.*111T>G
|
ENSP00000456302.1:n.*111T>G
|
|
ENST00000570076.5:c.*310T>G
|
ENSP00000456961.1:n.*310T>G
|
|
NM_000303.2:c.*111T>G
|
NP_000294.1:n.*111T>G
|
|
XM_005255374.3:c.*111T>G
|
XP_005255431.1:n.*111T>G
|
|
XM_011522538.1:c.640-7098T>G
|
XP_011520840.1:n.640-7098T>G
|
|
XM_005255374.4:c.*111T>G
|
XP_005255431.1:n.*111T>G
|
|
NM_000303.3:c.*111T>G
MANE Select
|
NP_000294.1:n.*111T>G
|
|