|
NM_018979.4:c.2624C>G
MANE Select
|
NP_061852.3:p.Thr875Arg
|
|
ENST00000315939.11:c.2624C>G
MANE Select
|
ENSP00000313059.6:p.Thr875Arg
|
|
NM_213655.5:c.3867+1462C>G
MANE Plus Clinical
|
NP_998820.3:n.3867+1462C>G
|
|
ENST00000340908.9:c.3867+1462C>G
MANE Plus Clinical
|
ENSP00000341292.5:n.3867+1462C>G
|
|
NM_001184985.1:c.3613-898C>G
|
NP_001171914.1:n.3613-898C>G
|
|
NM_001184985.2:c.3613-898C>G
|
NP_001171914.1:n.3613-898C>G
|
|
NM_014823.2:c.2370+1462C>G
|
NP_055638.2:n.2370+1462C>G
|
|
NM_014823.3:c.2370+1462C>G
|
NP_055638.2:n.2370+1462C>G
|
|
NM_018979.3:c.2624C>G
|
NP_061852.3:p.Thr875Arg
|
|
NM_213655.4:c.3867+1462C>G
|
NP_998820.3:n.3867+1462C>G
|
|
ENST00000315939.10:c.2624C>G
|
ENSP00000313059.6:p.Thr875Arg
|
|
ENST00000340908.8:c.3867+1462C>G
|
ENSP00000341292.5:n.3867+1462C>G
|
|
ENST00000530271.6:c.3863C>G
|
ENSP00000433548.3:p.Thr1288Arg
|
|
ENST00000535572.5:c.2370+1462C>G
|
ENSP00000441972.1:n.2370+1462C>G
|
|
ENST00000535698.1:c.434C>G
|
ENSP00000439552.1:p.Thr145Arg
|
|
ENST00000537687.5:c.3613-898C>G
|
ENSP00000444465.1:n.3613-898C>G
|
|
ENST00000542543.1:n.347+1462C>G
|
|
|
ENST00000544965.5:c.340+1462C>G
|
|
|
ENST00000545285.5:c.332-898C>G
|
|
|
ENST00000674810.1:n.3221C>G
|
|
|
ENST00000675236.1:n.1519C>G
|
|
|
ENST00000675631.1:c.1403C>G
|
ENSP00000502415.1:p.Thr468Arg
|
|
ENST00000676347.1:c.558+1462C>G
|
ENSP00000501875.1:n.558+1462C>G
|
|
XM_006719003.1:c.2621C>G
|
XP_006719066.1:p.Thr874Arg
|
|
XM_006719003.2:c.2621C>G
|
XP_006719066.1:p.Thr874Arg
|
|
XM_011520997.1:c.3863C>G
|
XP_011519299.1:p.Thr1288Arg
|
|
XM_011520997.3:c.3863C>G
|
XP_011519299.1:p.Thr1288Arg
|
|
XM_011520998.1:c.3860C>G
|
XP_011519300.1:p.Thr1287Arg
|
|
XM_011520998.2:c.3860C>G
|
XP_011519300.1:p.Thr1287Arg
|
|
XM_011520999.1:c.3863C>G
|
XP_011519301.1:p.Thr1288Arg
|
|
XM_011520999.2:c.3863C>G
|
XP_011519301.1:p.Thr1288Arg
|
|
XM_011521000.1:c.3863C>G
|
XP_011519302.1:p.Thr1288Arg
|
|
XM_011521000.2:c.3863C>G
|
XP_011519302.1:p.Thr1288Arg
|
|
XM_011521001.1:c.3863C>G
|
XP_011519303.1:p.Thr1288Arg
|
|
XM_011521001.2:c.3863C>G
|
XP_011519303.1:p.Thr1288Arg
|
|
XM_011521002.1:c.3610-898C>G
|
XP_011519304.1:n.3610-898C>G
|
|
XM_011521002.2:c.3610-898C>G
|
XP_011519304.1:n.3610-898C>G
|
|
XM_011521003.1:c.3612+1462C>G
|
XP_011519305.1:n.3612+1462C>G
|
|
XM_011521003.2:c.3612+1462C>G
|
XP_011519305.1:n.3612+1462C>G
|
|
XM_011521004.1:c.3609+1462C>G
|
XP_011519306.1:n.3609+1462C>G
|
|
XM_011521004.2:c.3609+1462C>G
|
XP_011519306.1:n.3609+1462C>G
|
|
XM_011521005.1:c.2642C>G
|
XP_011519307.1:p.Thr881Arg
|
|
XM_011521005.2:c.2642C>G
|
XP_011519307.1:p.Thr881Arg
|
|
XM_011521006.1:c.2540C>G
|
XP_011519308.1:p.Thr847Arg
|
|
XM_011521006.2:c.2540C>G
|
XP_011519308.1:p.Thr847Arg
|
|
XM_011521007.1:c.2537C>G
|
XP_011519309.1:p.Thr846Arg
|
|
XM_011521007.2:c.2537C>G
|
XP_011519309.1:p.Thr846Arg
|
|
XM_011521008.1:c.2289+1462C>G
|
XP_011519310.1:n.2289+1462C>G
|
|
XM_011521008.2:c.2289+1462C>G
|
XP_011519310.1:n.2289+1462C>G
|
|
XM_011521009.1:c.2286+1462C>G
|
XP_011519311.1:n.2286+1462C>G
|
|
XM_011521009.2:c.2286+1462C>G
|
XP_011519311.1:n.2286+1462C>G
|
|
XM_017019834.1:c.2371-898C>G
|
XP_016875323.1:n.2371-898C>G
|
|
XM_017019835.1:c.2290-898C>G
|
XP_016875324.1:n.2290-898C>G
|
|
XM_017019836.1:c.2287-898C>G
|
XP_016875325.1:n.2287-898C>G
|
|
XM_017019837.1:c.2373+1462C>G
|
XP_016875326.1:n.2373+1462C>G
|
|
XM_017019838.1:c.2370+1462C>G
|
XP_016875327.1:n.2370+1462C>G
|
|
XM_017019839.1:c.2289+1462C>G
|
XP_016875328.1:n.2289+1462C>G
|
