ENST00000492931.6:n.1144A>C
(ADA)
|
|
|
ENST00000536076.2:c.824A>C
(ADA)
|
ENSP00000512234.1:p.Asn275Thr
|
|
ENST00000536532.6:c.*120A>C
(ADA)
|
ENSP00000440946.1:n.*120A>C
|
|
ENST00000537820.2:c.905A>C
(ADA)
|
ENSP00000441818.1:p.Asn302Thr
|
|
ENST00000539235.6:c.*361A>C
(ADA)
|
ENSP00000446464.1:n.*361A>C
|
|
ENST00000695889.1:c.452A>C
(ADA)
|
ENSP00000512240.1:p.Asn151Thr
|
|
ENST00000695890.1:n.5088A>C
(ADA)
|
|
|
ENST00000695891.1:c.517A>C
(ADA)
|
ENSP00000512241.1:n.517A>C
|
|
ENST00000695927.1:c.1055A>C
(ADA)
|
ENSP00000512270.1:p.Asn352Thr
|
|
ENST00000695949.1:c.902A>C
(ADA)
|
ENSP00000512281.1:p.Asn301Thr
|
|
ENST00000695956.1:c.132A>C
(ADA)
|
|
|
ENST00000695957.1:c.*468A>C
(ADA)
|
ENSP00000512286.1:n.*468A>C
|
|
ENST00000695991.1:c.515A>C
(ADA)
|
ENSP00000512314.1:p.Asn172Thr
|
|
ENST00000695992.1:c.*120A>C
(ADA)
|
ENSP00000512315.1:n.*120A>C
|
|
ENST00000695993.1:c.977A>C
(ADA)
|
ENSP00000512316.1:p.Asn326Thr
|
|
ENST00000695994.1:c.*120A>C
(ADA)
|
ENSP00000512317.1:n.*120A>C
|
|
ENST00000695995.1:c.587A>C
(ADA)
|
ENSP00000512318.1:p.Asn196Thr
|
|
ENST00000695996.1:n.1059A>C
(ADA)
|
|
|
ENST00000696003.1:n.2761A>C
(ADA)
|
|
|
ENST00000696004.1:n.1761A>C
(ADA)
|
|
|
ENST00000696005.1:c.427A>C
(ADA)
|
|
|
ENST00000696006.1:c.*120A>C
(ADA)
|
ENSP00000512325.1:n.*120A>C
|
|
ENST00000696007.1:c.904A>C
(ADA)
|
ENSP00000512326.1:n.904A>C
|
|
ENST00000696008.1:n.3331A>C
(ADA)
|
|
|
ENST00000696017.1:c.974A>C
(ADA)
|
ENSP00000512333.1:p.Asn325Thr
|
|
ENST00000696034.1:c.*120A>C
(ADA)
|
ENSP00000512343.1:n.*120A>C
|
|
ENST00000696035.1:n.1163A>C
(ADA)
|
|
|
ENST00000696036.1:n.1678A>C
(ADA)
|
|
|
ENST00000696037.1:n.2654A>C
(ADA)
|
|
|
ENST00000696038.1:c.*734A>C
(ADA)
|
ENSP00000512344.1:n.*734A>C
|
|
ENST00000696039.1:n.1341A>C
(ADA)
|
|
|
ENST00000696058.1:c.974A>C
(ADA)
|
ENSP00000512361.1:p.Asn325Thr
|
|
ENST00000696059.1:c.*922A>C
(ADA)
|
ENSP00000512362.1:n.*922A>C
|
|
ENST00000696060.1:c.1046A>C
(ADA)
|
ENSP00000512363.1:p.Asn349Thr
|
|
ENST00000696061.1:c.974A>C
(ADA)
|
ENSP00000512364.1:p.Asn325Thr
|
|
ENST00000696062.1:c.1040A>C
(ADA)
|
ENSP00000512365.1:p.Asn347Thr
|
|
ENST00000696063.1:c.1052A>C
(ADA)
|
ENSP00000512366.1:p.Asn351Thr
|
|
ENST00000696064.1:c.824A>C
(ADA)
|
ENSP00000512367.1:p.Asn275Thr
|
|
ENST00000696065.1:c.299A>C
(ADA)
|
ENSP00000512368.1:p.Asn100Thr
|
|
ENST00000696072.1:n.332A>C
(ADA)
|
|
|
ENST00000696073.1:n.1288A>C
(ADA)
|
|
|
ENST00000696074.1:n.528A>C
(ADA)
|
|
|
ENST00000696075.1:c.*947A>C
(ADA)
|
ENSP00000512374.1:n.*947A>C
|
|
ENST00000696076.1:c.1046A>C
(ADA)
|
ENSP00000512375.1:p.Asn349Thr
|
|
ENST00000696077.1:c.971A>C
(ADA)
|
ENSP00000512376.1:p.Asn324Thr
|
|
ENST00000696078.1:c.974A>C
(ADA)
|
ENSP00000512377.1:p.Asn325Thr
|
|
ENST00000696079.1:c.974A>C
(ADA)
|
ENSP00000512378.1:p.Asn325Thr
|
|
ENST00000696080.1:c.977A>C
(ADA)
|
ENSP00000512379.1:p.Asn326Thr
|
|
ENST00000696081.1:n.1096A>C
(ADA)
|
|
|
ENST00000696082.1:c.1052A>C
(ADA)
|
ENSP00000512380.1:p.Asn351Thr
|
|
ENST00000696083.1:n.1934A>C
(ADA)
|
|
|
ENST00000696084.1:n.1154A>C
(ADA)
|
|
|
ENST00000696104.1:c.*46A>C
(ADA)
|
ENSP00000512399.1:n.*46A>C
|
|
ENST00000372874.9:c.977A>C
(ADA)
MANE Select
|
ENSP00000361965.4:p.Asn326Thr
|
|
ENST00000372874.8:c.977A>C
(ADA)
|
ENSP00000361965.4:p.Asn326Thr
|
|
ENST00000372887.5:c.152-3533T>G
(PKIG)
|
ENSP00000361978.1:n.152-3533T>G
|
|
ENST00000464097.5:n.1343A>C
(ADA)
|
|
|
ENST00000492931.5:n.1137A>C
(ADA)
|
|
|
ENST00000536532.5:c.*120A>C
(ADA)
|
ENSP00000440946.1:n.*120A>C
|
|
ENST00000537820.1:c.905A>C
(ADA)
|
ENSP00000441818.1:p.Asn302Thr
|
|
ENST00000539235.5:c.*361A>C
(ADA)
|
ENSP00000446464.1:n.*361A>C
|
|
NM_000022.2:c.977A>C , LRG_16t1:c.977A>C
(ADA)
|
NP_000013.2:p.Asn326Thr
|
|
XM_005260236.2:c.905A>C
(ADA)
|
XP_005260293.1:p.Asn302Thr
|
|
XM_011528478.1:c.572A>C
(ADA)
|
XP_011526780.1:p.Asn191Thr
|
|
XM_011528479.1:c.572A>C
(ADA)
|
XP_011526781.1:p.Asn191Thr
|
|
XR_244129.1:n.966A>C
(ADA)
|
|
|
NM_000022.3:c.977A>C
(ADA)
|
NP_000013.2:p.Asn326Thr
|
|
NM_001322050.1:c.572A>C
(ADA)
|
NP_001308979.1:p.Asn191Thr
|
|
NM_001322051.1:c.905A>C
(ADA)
|
NP_001308980.1:p.Asn302Thr
|
|
NR_136160.1:n.1063A>C
(ADA)
|
|
|
NM_000022.4:c.977A>C
(ADA)
MANE Select
|
NP_000013.2:p.Asn326Thr
|
|
NM_001322050.2:c.572A>C
(ADA)
|
NP_001308979.1:p.Asn191Thr
|
|
NM_001322051.2:c.905A>C
(ADA)
|
NP_001308980.1:p.Asn302Thr
|
|
NR_136160.2:n.1004A>C
(ADA)
|
|
|