|
ENST00000524561.2:n.3739A>G
|
|
|
|
ENST00000528374.2:c.729A>G
|
|
|
|
ENST00000529967.6:n.2477A>G
|
|
|
|
ENST00000532220.2:n.3371A>G
|
|
|
|
ENST00000642611.2:n.5338A>G
|
|
|
|
ENST00000644057.2:n.581A>G
|
|
|
|
ENST00000645004.2:n.1637A>G
|
|
|
|
ENST00000682051.1:n.4300A>G
|
|
|
|
ENST00000682110.1:n.4353A>G
|
|
|
|
ENST00000682140.1:c.4004A>G
|
ENSP00000507829.1:p.His1335Arg
|
|
|
ENST00000682185.1:n.5443A>G
|
|
|
|
ENST00000682204.1:c.*2276A>G
|
ENSP00000507094.1:n.*2276A>G
|
|
|
ENST00000682215.1:n.4720A>G
|
|
|
|
ENST00000682288.1:c.*2569A>G
|
ENSP00000507506.1:n.*2569A>G
|
|
|
ENST00000682442.1:n.4573A>G
|
|
|
|
ENST00000682528.1:n.4430A>G
|
|
|
|
ENST00000682673.1:n.4297A>G
|
|
|
|
ENST00000682805.1:n.4758A>G
|
|
|
|
ENST00000682965.1:c.*560A>G
|
ENSP00000508229.1:n.*560A>G
|
|
|
ENST00000683093.1:n.5437A>G
|
|
|
|
ENST00000683136.1:c.4021A>G
|
ENSP00000507768.1:p.Thr1341Ala
|
|
|
ENST00000683153.1:n.4395A>G
|
|
|
|
ENST00000683365.1:n.4455A>G
|
|
|
|
ENST00000683377.1:n.4353A>G
|
|
|
|
ENST00000683456.1:c.*1275A>G
|
ENSP00000508318.1:n.*1275A>G
|
|
|
ENST00000683522.1:n.4353A>G
|
|
|
|
ENST00000683562.1:c.*2307A>G
|
ENSP00000508265.1:n.*2307A>G
|
|
|
ENST00000683693.1:n.5785A>G
|
|
|
|
ENST00000683725.1:c.4138A>G
|
ENSP00000507496.1:p.Thr1380Ala
|
|
|
ENST00000684010.1:n.4348A>G
|
|
|
|
ENST00000684157.1:n.5338A>G
|
|
|
|
ENST00000684253.1:n.4256A>G
|
|
|
|
ENST00000684288.1:c.*2310A>G
|
ENSP00000507143.1:n.*2310A>G
|
|
|
ENST00000684313.1:n.3785A>G
|
|
|
|
ENST00000684332.1:n.4426A>G
|
|
|
|
ENST00000684371.1:n.4459A>G
|
|
|
|
ENST00000684404.1:n.5381A>G
|
|
|
|
ENST00000684442.1:n.4577A>G
|
|
|
|
ENST00000684555.1:c.*2350A>G
|
ENSP00000507705.1:n.*2350A>G
|
|
|
ENST00000684571.1:c.3979A>G
|
ENSP00000506935.1:p.Thr1327Ala
|
|
|
ENST00000684593.1:c.*3843A>G
|
ENSP00000507005.1:n.*3843A>G
|
|
|
ENST00000684711.1:c.*2534A>G
|
ENSP00000506841.1:n.*2534A>G
|
|
|
ENST00000302539.9:c.4141A>G
|
ENSP00000303960.4:p.Thr1381Ala
|
|
|
ENST00000389817.8:c.4138A>G
MANE Select
|
ENSP00000374467.4:p.Thr1380Ala
|
|
|
ENST00000642271.1:c.4135A>G
|
ENSP00000493749.1:p.Thr1379Ala
|
|
|
ENST00000642579.1:c.2192A>G
|
|
|
|
ENST00000642611.1:n.5223A>G
|
|
|
|
ENST00000642902.1:c.3920A>G
|
|
|
|
ENST00000643260.1:c.4138A>G
|
ENSP00000494450.1:p.Thr1380Ala
|
|
|
ENST00000643562.1:c.*2260A>G
|
ENSP00000496124.1:n.*2260A>G
|
|
|
ENST00000643925.1:c.2778A>G
|
|
|
|
ENST00000644057.1:n.215A>G
|
|
|
|
ENST00000644484.1:c.*3524A>G
|
ENSP00000493558.1:n.*3524A>G
|
|
|
ENST00000644675.1:c.*2310A>G
|
ENSP00000494567.1:n.*2310A>G
|
|
|
ENST00000644757.1:c.*3202+352A>G
|
ENSP00000495085.1:n.*3202+352A>G
|
|
|
ENST00000644772.1:c.4204A>G
|
ENSP00000494321.1:p.Thr1402Ala
|
|
|
ENST00000645004.1:n.1831A>G
|
|
|
|
ENST00000645076.1:c.3337A>G
|
|
|
|
ENST00000645417.1:c.1326A>G
|
|
|
|
ENST00000645744.1:c.*3903A>G
|
ENSP00000494564.1:n.*3903A>G
|
|
|
ENST00000645760.1:c.4559A>G
|
|
|
|
ENST00000645884.1:c.*1421A>G
|
ENSP00000495516.1:n.*1421A>G
|
|
|
ENST00000646003.1:c.*2240A>G
|
ENSP00000495259.1:n.*2240A>G
|
|
|
ENST00000646207.1:c.*2975A>G
|
ENSP00000495025.1:n.*2975A>G
|
|
|
ENST00000646276.1:c.*3542A>G
|
ENSP00000496070.1:n.*3542A>G
|
|
|
ENST00000646592.1:c.3444A>G
|
|
|
|
ENST00000646902.1:c.4105A>G
|
ENSP00000494101.1:p.Thr1369Ala
|
|
|
ENST00000646993.1:c.*2680A>G
|
ENSP00000493720.1:n.*2680A>G
|
|
|
ENST00000647013.1:c.4144A>G
|
ENSP00000496741.1:n.4144A>G
|
|
|
ENST00000647015.1:c.3889A>G
|
ENSP00000495389.1:p.Thr1297Ala
|
|
|
ENST00000647086.1:c.*3724A>G
|
ENSP00000493677.1:n.*3724A>G
|
|
|
ENST00000647158.1:c.*2425A>G
|
ENSP00000495744.1:n.*2425A>G
|
|
|
ENST00000302539.8:c.4141A>G
|
ENSP00000303960.4:p.Thr1381Ala
|
|
|
ENST00000389817.7:c.4138A>G
|
ENSP00000374467.3:p.Thr1380Ala
|
|
|
ENST00000525022.1:n.4A>G
|
|
|
|
ENST00000526168.5:c.6A>G
|
|
|
|
NM_000352.4:c.4138A>G
|
NP_000343.2:p.Thr1380Ala
|
|
|
NM_001287174.1:c.4141A>G
|
NP_001274103.1:p.Thr1381Ala
|
|
|
XM_011520331.1:c.4138A>G
|
XP_011518633.1:p.Thr1380Ala
|
|
|
XM_011520332.1:c.4141A>G
|
XP_011518634.1:p.Thr1381Ala
|
|
|
XM_011520333.1:c.2638A>G
|
XP_011518635.1:p.Thr880Ala
|
|
|
XR_930890.1:n.4204A>G
|
|
|
|
NM_001351295.1:c.4204A>G
|
NP_001338224.1:p.Thr1402Ala
|
|
|
NM_001351296.1:c.4138A>G
|
NP_001338225.1:p.Thr1380Ala
|
|
|
NM_001351297.1:c.4135A>G
|
NP_001338226.1:p.Thr1379Ala
|
|
|
NR_147094.1:n.4433A>G
|
|
|
|
XM_017018197.2:c.4207A>G
|
XP_016873686.1:p.Thr1403Ala
|
|
|
XM_017018199.1:c.4204A>G
|
XP_016873688.1:p.Thr1402Ala
|
|
|
XM_017018201.2:c.4207A>G
|
XP_016873690.1:p.Thr1403Ala
|
|
|
XM_017018202.1:c.2704A>G
|
XP_016873691.1:p.Thr902Ala
|
|
|
XM_017018204.1:c.2095A>G
|
XP_016873693.1:p.Thr699Ala
|
|
|
XM_024448668.1:c.2506A>G
|
XP_024304436.1:p.Thr836Ala
|
|
|
XR_001747945.2:n.4279A>G
|
|
|
|
XR_001747946.2:n.4210A>G
|
|
|
|
XR_002957189.1:n.5860A>G
|
|
|
|
NM_000352.6:c.4138A>G
MANE Select
|
NP_000343.2:p.Thr1380Ala
|
|
|
NM_001287174.2:c.4141A>G
|
NP_001274103.1:p.Thr1381Ala
|
|
|
NM_001351295.2:c.4204A>G
|
NP_001338224.1:p.Thr1402Ala
|
|
|
NM_001351296.2:c.4138A>G
|
NP_001338225.1:p.Thr1380Ala
|
|
|
NM_001351297.2:c.4135A>G
|
NP_001338226.1:p.Thr1379Ala
|
|
|
NR_147094.2:n.4433A>G
|
|
|
|
NM_001287174.3:c.4141A>G
|
NP_001274103.1:p.Thr1381Ala
|
|
