ENST00000567697.2:n.4025A>G
|
|
|
ENST00000682393.1:c.*258-1428A>G
|
ENSP00000506774.1:n.*258-1428A>G
|
|
ENST00000683094.1:c.*262-1428A>G
|
ENSP00000508230.1:n.*262-1428A>G
|
|
ENST00000683274.1:c.*180-1428A>G
|
ENSP00000507262.1:n.*180-1428A>G
|
|
ENST00000683435.1:c.*753A>G
|
ENSP00000508092.1:n.*753A>G
|
|
ENST00000268261.9:c.*116A>G
MANE Select
|
ENSP00000268261.4:n.*116A>G
|
|
ENST00000268261.8:c.*116A>G
|
ENSP00000268261.4:n.*116A>G
|
|
ENST00000562025.1:n.391A>G
|
|
|
ENST00000562318.5:c.*579A>G
|
ENSP00000454395.1:n.*579A>G
|
|
ENST00000565221.5:c.*475A>G
|
ENSP00000457932.1:n.*475A>G
|
|
ENST00000566540.5:c.*479A>G
|
ENSP00000454284.1:n.*479A>G
|
|
ENST00000566604.5:c.*397A>G
|
ENSP00000456774.1:n.*397A>G
|
|
ENST00000567697.1:n.4025A>G
|
|
|
ENST00000569958.5:c.*116A>G
|
ENSP00000456302.1:n.*116A>G
|
|
ENST00000570076.5:c.*315A>G
|
ENSP00000456961.1:n.*315A>G
|
|
NM_000303.2:c.*116A>G
|
NP_000294.1:n.*116A>G
|
|
XM_005255374.3:c.*116A>G
|
XP_005255431.1:n.*116A>G
|
|
XM_011522538.1:c.640-7093A>G
|
XP_011520840.1:n.640-7093A>G
|
|
XM_005255374.4:c.*116A>G
|
XP_005255431.1:n.*116A>G
|
|
NM_000303.3:c.*116A>G
MANE Select
|
NP_000294.1:n.*116A>G
|
|