ENST00000492931.6:n.1151T>C
(ADA)
|
|
|
ENST00000536076.2:c.831T>C
(ADA)
|
ENSP00000512234.1:p.Asn277=
|
|
ENST00000536532.6:c.*127T>C
(ADA)
|
ENSP00000440946.1:n.*127T>C
|
|
ENST00000537820.2:c.912T>C
(ADA)
|
ENSP00000441818.1:p.Asn304=
|
|
ENST00000539235.6:c.*368T>C
(ADA)
|
ENSP00000446464.1:n.*368T>C
|
|
ENST00000695889.1:c.459T>C
(ADA)
|
ENSP00000512240.1:p.Asn153=
|
|
ENST00000695890.1:n.5095T>C
(ADA)
|
|
|
ENST00000695891.1:c.524T>C
(ADA)
|
ENSP00000512241.1:n.524T>C
|
|
ENST00000695927.1:c.1062T>C
(ADA)
|
ENSP00000512270.1:p.Asn354=
|
|
ENST00000695949.1:c.909T>C
(ADA)
|
ENSP00000512281.1:p.Asn303=
|
|
ENST00000695956.1:c.139T>C
(ADA)
|
|
|
ENST00000695957.1:c.*475T>C
(ADA)
|
ENSP00000512286.1:n.*475T>C
|
|
ENST00000695991.1:c.522T>C
(ADA)
|
ENSP00000512314.1:p.Asn174=
|
|
ENST00000695992.1:c.*127T>C
(ADA)
|
ENSP00000512315.1:n.*127T>C
|
|
ENST00000695993.1:c.984T>C
(ADA)
|
ENSP00000512316.1:p.Asn328=
|
|
ENST00000695994.1:c.*127T>C
(ADA)
|
ENSP00000512317.1:n.*127T>C
|
|
ENST00000695995.1:c.594T>C
(ADA)
|
ENSP00000512318.1:p.Asn198=
|
|
ENST00000695996.1:n.1066T>C
(ADA)
|
|
|
ENST00000696003.1:n.2768T>C
(ADA)
|
|
|
ENST00000696004.1:n.1768T>C
(ADA)
|
|
|
ENST00000696005.1:c.434T>C
(ADA)
|
|
|
ENST00000696006.1:c.*127T>C
(ADA)
|
ENSP00000512325.1:n.*127T>C
|
|
ENST00000696007.1:c.911T>C
(ADA)
|
ENSP00000512326.1:n.911T>C
|
|
ENST00000696008.1:n.3338T>C
(ADA)
|
|
|
ENST00000696017.1:c.981T>C
(ADA)
|
ENSP00000512333.1:p.Asn327=
|
|
ENST00000696034.1:c.*127T>C
(ADA)
|
ENSP00000512343.1:n.*127T>C
|
|
ENST00000696035.1:n.1170T>C
(ADA)
|
|
|
ENST00000696036.1:n.1685T>C
(ADA)
|
|
|
ENST00000696037.1:n.2661T>C
(ADA)
|
|
|
ENST00000696038.1:c.*741T>C
(ADA)
|
ENSP00000512344.1:n.*741T>C
|
|
ENST00000696039.1:n.1348T>C
(ADA)
|
|
|
ENST00000696058.1:c.981T>C
(ADA)
|
ENSP00000512361.1:p.Asn327=
|
|
ENST00000696059.1:c.*929T>C
(ADA)
|
ENSP00000512362.1:n.*929T>C
|
|
ENST00000696060.1:c.1053T>C
(ADA)
|
ENSP00000512363.1:p.Asn351=
|
|
ENST00000696061.1:c.981T>C
(ADA)
|
ENSP00000512364.1:p.Asn327=
|
|
ENST00000696062.1:c.1047T>C
(ADA)
|
ENSP00000512365.1:p.Asn349=
|
|
ENST00000696063.1:c.1059T>C
(ADA)
|
ENSP00000512366.1:p.Asn353=
|
|
ENST00000696064.1:c.831T>C
(ADA)
|
ENSP00000512367.1:p.Asn277=
|
|
ENST00000696065.1:c.306T>C
(ADA)
|
ENSP00000512368.1:p.Asn102=
|
|
ENST00000696072.1:n.339T>C
(ADA)
|
|
|
ENST00000696073.1:n.1295T>C
(ADA)
|
|
|
ENST00000696074.1:n.535T>C
(ADA)
|
|
|
ENST00000696075.1:c.*954T>C
(ADA)
|
ENSP00000512374.1:n.*954T>C
|
|
ENST00000696076.1:c.1053T>C
(ADA)
|
ENSP00000512375.1:p.Asn351=
|
|
ENST00000696077.1:c.978T>C
(ADA)
|
ENSP00000512376.1:p.Asn326=
|
|
ENST00000696078.1:c.981T>C
(ADA)
|
ENSP00000512377.1:p.Asn327=
|
|
ENST00000696079.1:c.981T>C
(ADA)
|
ENSP00000512378.1:p.Asn327=
|
|
ENST00000696080.1:c.984T>C
(ADA)
|
ENSP00000512379.1:p.Asn328=
|
|
ENST00000696081.1:n.1103T>C
(ADA)
|
|
|
ENST00000696082.1:c.1059T>C
(ADA)
|
ENSP00000512380.1:p.Asn353=
|
|
ENST00000696083.1:n.1941T>C
(ADA)
|
|
|
ENST00000696084.1:n.1161T>C
(ADA)
|
|
|
ENST00000696104.1:c.*53T>C
(ADA)
|
ENSP00000512399.1:n.*53T>C
|
|
ENST00000372874.9:c.984T>C
(ADA)
MANE Select
|
ENSP00000361965.4:p.Asn328=
|
|
ENST00000372874.8:c.984T>C
(ADA)
|
ENSP00000361965.4:p.Asn328=
|
|
ENST00000372887.5:c.152-3540A>G
(PKIG)
|
ENSP00000361978.1:n.152-3540A>G
|
|
ENST00000464097.5:n.1350T>C
(ADA)
|
|
|
ENST00000492931.5:n.1144T>C
(ADA)
|
|
|
ENST00000536532.5:c.*127T>C
(ADA)
|
ENSP00000440946.1:n.*127T>C
|
|
ENST00000537820.1:c.912T>C
(ADA)
|
ENSP00000441818.1:p.Asn304=
|
|
ENST00000539235.5:c.*368T>C
(ADA)
|
ENSP00000446464.1:n.*368T>C
|
|
NM_000022.2:c.984T>C , LRG_16t1:c.984T>C
(ADA)
|
NP_000013.2:p.Asn328=
|
|
XM_005260236.2:c.912T>C
(ADA)
|
XP_005260293.1:p.Asn304=
|
|
XM_011528478.1:c.579T>C
(ADA)
|
XP_011526780.1:p.Asn193=
|
|
XM_011528479.1:c.579T>C
(ADA)
|
XP_011526781.1:p.Asn193=
|
|
XR_244129.1:n.973T>C
(ADA)
|
|
|
NM_000022.3:c.984T>C
(ADA)
|
NP_000013.2:p.Asn328=
|
|
NM_001322050.1:c.579T>C
(ADA)
|
NP_001308979.1:p.Asn193=
|
|
NM_001322051.1:c.912T>C
(ADA)
|
NP_001308980.1:p.Asn304=
|
|
NR_136160.1:n.1070T>C
(ADA)
|
|
|
NM_000022.4:c.984T>C
(ADA)
MANE Select
|
NP_000013.2:p.Asn328=
|
|
NM_001322050.2:c.579T>C
(ADA)
|
NP_001308979.1:p.Asn193=
|
|
NM_001322051.2:c.912T>C
(ADA)
|
NP_001308980.1:p.Asn304=
|
|
NR_136160.2:n.1011T>C
(ADA)
|
|
|