ENST00000478003.2:n.2171G>C
|
|
|
ENST00000682276.1:n.1788G>C
|
|
|
ENST00000682892.1:c.1890G>C
|
ENSP00000507214.1:p.Glu630Asp
|
|
ENST00000682952.1:n.1982G>C
|
|
|
ENST00000684455.1:c.1556G>C
|
|
|
ENST00000684642.1:c.1740G>C
|
ENSP00000507355.1:p.Glu580Asp
|
|
ENST00000684740.1:n.2521G>C
|
|
|
ENST00000303236.9:c.2343G>C
MANE Select
|
ENSP00000307235.3:p.Glu781Asp
|
|
ENST00000652099.1:c.2537G>C
|
|
|
ENST00000652736.1:n.2219G>C
|
|
|
ENST00000303236.7:c.2343G>C
|
ENSP00000307235.3:p.Glu781Asp
|
|
ENST00000415570.1:c.1980G>C
|
ENSP00000412076.1:p.Glu660Asp
|
|
ENST00000419748.5:c.1890G>C
|
ENSP00000408325.1:p.Glu630Asp
|
|
ENST00000470706.1:n.49-63G>C
|
|
|
NM_001313915.1:c.1890G>C
|
NP_001300844.1:p.Glu630Asp
|
|
NM_004836.5:c.2343G>C
|
NP_004827.4:p.Glu781Asp
|
|
NM_004836.6:c.2343G>C
|
NP_004827.4:p.Glu781Asp
|
|
NR_110236.1:n.1277C>G
|
|
|
XM_005264649.3:c.1659G>C
|
XP_005264706.1:p.Glu553Asp
|
|
XM_017005376.2:c.1659G>C
|
XP_016860865.1:p.Glu553Asp
|
|
NM_004836.7:c.2343G>C
MANE Select
|
NP_004827.4:p.Glu781Asp
|
|
NM_001313915.2:c.1890G>C
|
NP_001300844.1:p.Glu630Asp
|
|