ENST00000492931.6:n.883G>A
(ADA)
|
|
|
ENST00000536076.2:c.563G>A
(ADA)
|
ENSP00000512234.1:p.Gly188Asp
|
|
ENST00000536532.6:c.716G>A
(ADA)
|
ENSP00000440946.1:p.Gly239Asp
|
|
ENST00000537820.2:c.644G>A
(ADA)
|
ENSP00000441818.1:p.Gly215Asp
|
|
ENST00000539235.6:c.*100G>A
(ADA)
|
ENSP00000446464.1:n.*100G>A
|
|
ENST00000695889.1:c.256G>A
(ADA)
|
ENSP00000512240.1:p.Ala86Thr
|
|
ENST00000695890.1:n.2595G>A
(ADA)
|
|
|
ENST00000695891.1:c.256G>A
(ADA)
|
ENSP00000512241.1:p.Ala86Thr
|
|
ENST00000695927.1:c.794G>A
(ADA)
|
ENSP00000512270.1:p.Gly265Asp
|
|
ENST00000695949.1:c.641G>A
(ADA)
|
ENSP00000512281.1:p.Gly214Asp
|
|
ENST00000695957.1:c.*207G>A
(ADA)
|
ENSP00000512286.1:n.*207G>A
|
|
ENST00000695991.1:c.254G>A
(ADA)
|
ENSP00000512314.1:p.Gly85Asp
|
|
ENST00000695992.1:c.716G>A
(ADA)
|
ENSP00000512315.1:p.Gly239Asp
|
|
ENST00000695993.1:c.716G>A
(ADA)
|
ENSP00000512316.1:p.Gly239Asp
|
|
ENST00000695994.1:c.689G>A
(ADA)
|
ENSP00000512317.1:p.Gly230Asp
|
|
ENST00000695995.1:c.326G>A
(ADA)
|
ENSP00000512318.1:p.Gly109Asp
|
|
ENST00000695996.1:n.863G>A
(ADA)
|
|
|
ENST00000696003.1:n.884G>A
(ADA)
|
|
|
ENST00000696004.1:n.884G>A
(ADA)
|
|
|
ENST00000696005.1:c.166G>A
(ADA)
|
|
|
ENST00000696006.1:c.644G>A
(ADA)
|
ENSP00000512325.1:p.Gly215Asp
|
|
ENST00000696007.1:c.643G>A
(ADA)
|
ENSP00000512326.1:n.643G>A
|
|
ENST00000696008.1:n.3070G>A
(ADA)
|
|
|
ENST00000696017.1:c.713G>A
(ADA)
|
ENSP00000512333.1:p.Gly238Asp
|
|
ENST00000696034.1:c.716G>A
(ADA)
|
ENSP00000512343.1:p.Gly239Asp
|
|
ENST00000696035.1:n.902G>A
(ADA)
|
|
|
ENST00000696036.1:n.1482G>A
(ADA)
|
|
|
ENST00000696037.1:n.2393G>A
(ADA)
|
|
|
ENST00000696038.1:c.*538G>A
(ADA)
|
ENSP00000512344.1:n.*538G>A
|
|
ENST00000696039.1:n.1080G>A
(ADA)
|
|
|
ENST00000696058.1:c.713G>A
(ADA)
|
ENSP00000512361.1:p.Gly238Asp
|
|
ENST00000696059.1:c.*661G>A
(ADA)
|
ENSP00000512362.1:n.*661G>A
|
|
ENST00000696060.1:c.785G>A
(ADA)
|
ENSP00000512363.1:p.Gly262Asp
|
|
ENST00000696061.1:c.713G>A
(ADA)
|
ENSP00000512364.1:p.Gly238Asp
|
|
ENST00000696062.1:c.779G>A
(ADA)
|
ENSP00000512365.1:p.Gly260Asp
|
|
ENST00000696063.1:c.791G>A
(ADA)
|
ENSP00000512366.1:p.Gly264Asp
|
|
ENST00000696064.1:c.563G>A
(ADA)
|
ENSP00000512367.1:p.Gly188Asp
|
|
ENST00000696065.1:c.103G>A
(ADA)
|
ENSP00000512368.1:p.Ala35Thr
|
|
ENST00000696073.1:n.1027G>A
(ADA)
|
|
|
ENST00000696074.1:n.332G>A
(ADA)
|
|
|
ENST00000696075.1:c.*686G>A
(ADA)
|
ENSP00000512374.1:n.*686G>A
|
|
ENST00000696076.1:c.785G>A
(ADA)
|
ENSP00000512375.1:p.Gly262Asp
|
|
ENST00000696077.1:c.710G>A
(ADA)
|
ENSP00000512376.1:p.Gly237Asp
|
|
ENST00000696078.1:c.713G>A
(ADA)
|
ENSP00000512377.1:p.Gly238Asp
|
|
ENST00000696079.1:c.713G>A
(ADA)
|
ENSP00000512378.1:p.Gly238Asp
|
|
ENST00000696080.1:c.716G>A
(ADA)
|
ENSP00000512379.1:p.Gly239Asp
|
|
ENST00000696081.1:n.835G>A
(ADA)
|
|
|
ENST00000696082.1:c.791G>A
(ADA)
|
ENSP00000512380.1:p.Gly264Asp
|
|
ENST00000696083.1:n.1673G>A
(ADA)
|
|
|
ENST00000696084.1:n.893G>A
(ADA)
|
|
|
ENST00000696104.1:c.400G>A
(ADA)
|
ENSP00000512399.1:p.Ala134Thr
|
|
ENST00000372874.9:c.716G>A
(ADA)
MANE Select
|
ENSP00000361965.4:p.Gly239Asp
|
|
ENST00000372874.8:c.716G>A
(ADA)
|
ENSP00000361965.4:p.Gly239Asp
|
|
ENST00000372887.5:c.152-1040C>T
(PKIG)
|
ENSP00000361978.1:n.152-1040C>T
|
|
ENST00000464097.5:n.466G>A
(ADA)
|
|
|
ENST00000492931.5:n.876G>A
(ADA)
|
|
|
ENST00000536532.5:c.716G>A
(ADA)
|
ENSP00000440946.1:p.Gly239Asp
|
|
ENST00000537820.1:c.644G>A
(ADA)
|
ENSP00000441818.1:p.Gly215Asp
|
|
ENST00000539235.5:c.*100G>A
(ADA)
|
ENSP00000446464.1:n.*100G>A
|
|
NM_000022.2:c.716G>A , LRG_16t1:c.716G>A
(ADA)
|
NP_000013.2:p.Gly239Asp
|
|
XM_005260236.2:c.644G>A
(ADA)
|
XP_005260293.1:p.Gly215Asp
|
|
XM_011528478.1:c.311G>A
(ADA)
|
XP_011526780.1:p.Gly104Asp
|
|
XM_011528479.1:c.311G>A
(ADA)
|
XP_011526781.1:p.Gly104Asp
|
|
XR_244129.1:n.770G>A
(ADA)
|
|
|
NM_000022.3:c.716G>A
(ADA)
|
NP_000013.2:p.Gly239Asp
|
|
NM_001322050.1:c.311G>A
(ADA)
|
NP_001308979.1:p.Gly104Asp
|
|
NM_001322051.1:c.644G>A
(ADA)
|
NP_001308980.1:p.Gly215Asp
|
|
NR_136160.1:n.867G>A
(ADA)
|
|
|
NM_000022.4:c.716G>A
(ADA)
MANE Select
|
NP_000013.2:p.Gly239Asp
|
|
NM_001322050.2:c.311G>A
(ADA)
|
NP_001308979.1:p.Gly104Asp
|
|
NM_001322051.2:c.644G>A
(ADA)
|
NP_001308980.1:p.Gly215Asp
|
|
NR_136160.2:n.808G>A
(ADA)
|
|
|