ENST00000567697.2:n.4047T>A
|
|
|
ENST00000682393.1:c.*258-1406T>A
|
ENSP00000506774.1:n.*258-1406T>A
|
|
ENST00000683094.1:c.*262-1406T>A
|
ENSP00000508230.1:n.*262-1406T>A
|
|
ENST00000683274.1:c.*180-1406T>A
|
ENSP00000507262.1:n.*180-1406T>A
|
|
ENST00000683435.1:c.*775T>A
|
ENSP00000508092.1:n.*775T>A
|
|
ENST00000268261.9:c.*138T>A
MANE Select
|
ENSP00000268261.4:n.*138T>A
|
|
ENST00000268261.8:c.*138T>A
|
ENSP00000268261.4:n.*138T>A
|
|
ENST00000562025.1:n.413T>A
|
|
|
ENST00000562318.5:c.*601T>A
|
ENSP00000454395.1:n.*601T>A
|
|
ENST00000565221.5:c.*497T>A
|
ENSP00000457932.1:n.*497T>A
|
|
ENST00000566540.5:c.*501T>A
|
ENSP00000454284.1:n.*501T>A
|
|
ENST00000566604.5:c.*419T>A
|
ENSP00000456774.1:n.*419T>A
|
|
ENST00000567697.1:n.4047T>A
|
|
|
ENST00000569958.5:c.*138T>A
|
ENSP00000456302.1:n.*138T>A
|
|
ENST00000570076.5:c.*337T>A
|
ENSP00000456961.1:n.*337T>A
|
|
NM_000303.2:c.*138T>A
|
NP_000294.1:n.*138T>A
|
|
XM_005255374.3:c.*138T>A
|
XP_005255431.1:n.*138T>A
|
|
XM_011522538.1:c.640-7071T>A
|
XP_011520840.1:n.640-7071T>A
|
|
XM_005255374.4:c.*138T>A
|
XP_005255431.1:n.*138T>A
|
|
NM_000303.3:c.*138T>A
MANE Select
|
NP_000294.1:n.*138T>A
|
|