ENST00000698727.1:n.1297A>T
|
|
|
ENST00000698728.1:n.1816A>T
|
|
|
ENST00000698729.1:n.3362A>T
|
|
|
ENST00000698730.1:n.3362A>T
|
|
|
ENST00000698731.1:c.2096A>T
|
ENSP00000513898.1:p.Glu699Val
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|
ENST00000698732.1:c.*1098A>T
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ENSP00000513899.1:n.*1098A>T
|
|
ENST00000698733.1:c.*1424A>T
|
ENSP00000513900.1:n.*1424A>T
|
|
ENST00000698734.1:c.2237A>T
|
ENSP00000513901.1:p.Glu746Val
|
|
ENST00000698735.1:n.2352A>T
|
|
|
ENST00000698736.1:n.2352A>T
|
|
|
ENST00000698737.1:n.2352A>T
|
|
|
ENST00000698738.1:n.2352A>T
|
|
|
ENST00000698739.1:n.2352A>T
|
|
|
ENST00000372371.8:c.2237A>T
MANE Select
|
ENSP00000361446.3:p.Glu746Val
|
|
ENST00000372371.7:c.2237A>T
|
ENSP00000361446.3:p.Glu746Val
|
|
ENST00000472014.5:n.459A>T
|
|
|
ENST00000473588.2:c.900A>T
|
|
|
NM_007055.3:c.2237A>T
|
NP_008986.2:p.Glu746Val
|
|
NM_007055.4:c.2237A>T
MANE Select
|
NP_008986.2:p.Glu746Val
|
|