ENST00000478003.2:n.2287A>T
|
|
|
ENST00000682276.1:n.1904A>T
|
|
|
ENST00000682892.1:c.2006A>T
|
ENSP00000507214.1:p.Glu669Val
|
|
ENST00000682952.1:n.2098A>T
|
|
|
ENST00000684455.1:c.1672A>T
|
|
|
ENST00000684642.1:c.1856A>T
|
ENSP00000507355.1:p.Glu619Val
|
|
ENST00000684740.1:n.2637A>T
|
|
|
ENST00000303236.9:c.2459A>T
MANE Select
|
ENSP00000307235.3:p.Glu820Val
|
|
ENST00000652099.1:c.2653A>T
|
|
|
ENST00000652736.1:n.2335A>T
|
|
|
ENST00000303236.7:c.2459A>T
|
ENSP00000307235.3:p.Glu820Val
|
|
ENST00000415570.1:c.2096A>T
|
ENSP00000412076.1:p.Glu699Val
|
|
ENST00000419748.5:c.2006A>T
|
ENSP00000408325.1:p.Glu669Val
|
|
ENST00000470706.1:n.102A>T
|
|
|
NM_001313915.1:c.2006A>T
|
NP_001300844.1:p.Glu669Val
|
|
NM_004836.5:c.2459A>T
|
NP_004827.4:p.Glu820Val
|
|
NM_004836.6:c.2459A>T
|
NP_004827.4:p.Glu820Val
|
|
NR_110236.1:n.1161T>A
|
|
|
XM_005264649.3:c.1775A>T
|
XP_005264706.1:p.Glu592Val
|
|
XM_017005376.2:c.1775A>T
|
XP_016860865.1:p.Glu592Val
|
|
NM_004836.7:c.2459A>T
MANE Select
|
NP_004827.4:p.Glu820Val
|
|
NM_001313915.2:c.2006A>T
|
NP_001300844.1:p.Glu669Val
|
|