ENST00000698724.1:n.15A>T
|
|
|
ENST00000698727.1:n.1807A>T
|
|
|
ENST00000698728.1:n.2326A>T
|
|
|
ENST00000698729.1:n.3872A>T
|
|
|
ENST00000698730.1:n.3872A>T
|
|
|
ENST00000698731.1:c.2606A>T
|
ENSP00000513898.1:p.Asp869Val
|
|
ENST00000698732.1:c.*1608A>T
|
ENSP00000513899.1:n.*1608A>T
|
|
ENST00000698733.1:c.*1934A>T
|
ENSP00000513900.1:n.*1934A>T
|
|
ENST00000698734.1:c.*271A>T
|
ENSP00000513901.1:n.*271A>T
|
|
ENST00000698735.1:n.2862A>T
|
|
|
ENST00000698736.1:n.2862A>T
|
|
|
ENST00000698737.1:n.2862A>T
|
|
|
ENST00000698738.1:n.2862A>T
|
|
|
ENST00000698739.1:n.2862A>T
|
|
|
ENST00000372371.8:c.2747A>T
MANE Select
|
ENSP00000361446.3:p.Asp916Val
|
|
ENST00000372371.7:c.2747A>T
|
ENSP00000361446.3:p.Asp916Val
|
|
ENST00000472014.5:n.600A>T
|
|
|
NM_007055.3:c.2747A>T
|
NP_008986.2:p.Asp916Val
|
|
NM_007055.4:c.2747A>T
MANE Select
|
NP_008986.2:p.Asp916Val
|
|