ENST00000269571.10:c.3547G>T
MANE Select
|
ENSP00000269571.4:p.Asp1183Tyr
|
|
ENST00000269571.9:c.3547G>T
|
ENSP00000269571.4:p.Asp1183Tyr
|
|
ENST00000406381.6:c.3457G>T
|
ENSP00000385185.2:p.Asp1153Tyr
|
|
ENST00000445658.6:c.2719G>T
|
ENSP00000404047.2:p.Asp907Tyr
|
|
ENST00000541774.5:c.3502G>T
|
ENSP00000446466.1:p.Asp1168Tyr
|
|
ENST00000578373.5:c.*3337G>T
|
ENSP00000463427.1:n.*3337G>T
|
|
ENST00000584450.5:c.*126G>T
|
ENSP00000463714.1:n.*126G>T
|
|
ENST00000584601.5:c.3457G>T
|
ENSP00000462438.1:p.Asp1153Tyr
|
|
NM_001005862.2:c.3457G>T , LRG_724t1:c.3457G>T
|
NP_001005862.1:p.Asp1153Tyr
|
|
NM_001289936.1:c.3502G>T , LRG_724t4:c.3502G>T
|
NP_001276865.1:p.Asp1168Tyr
|
|
NM_001289937.1:c.*126G>T
|
NP_001276866.1:n.*126G>T
|
|
NM_004448.3:c.3547G>T , LRG_724t2:c.3547G>T
|
NP_004439.2:p.Asp1183Tyr
|
|
NR_110535.1:n.3871G>T
|
|
|
XM_024450641.1:c.3685G>T
|
XP_024306409.1:p.Asp1229Tyr
|
|
XM_024450642.1:c.3640G>T
|
XP_024306410.1:p.Asp1214Tyr
|
|
XM_024450643.1:c.3595G>T
|
XP_024306411.1:p.Asp1199Tyr
|
|
NM_001005862.3:c.3457G>T
|
NP_001005862.1:p.Asp1153Tyr
|
|
NM_001289936.2:c.3502G>T
|
NP_001276865.1:p.Asp1168Tyr
|
|
NM_001289937.2:c.*126G>T
|
NP_001276866.1:n.*126G>T
|
|
NM_001382782.1:c.3457G>T
|
NP_001369711.1:p.Asp1153Tyr
|
|
NM_001382783.1:c.3457G>T
|
NP_001369712.1:p.Asp1153Tyr
|
|
NM_001382784.1:c.3664G>T
|
NP_001369713.1:p.Asp1222Tyr
|
|
NM_001382785.1:c.3649G>T
|
NP_001369714.1:p.Asp1217Tyr
|
|
NM_001382786.1:c.3628G>T
|
NP_001369715.1:p.Asp1210Tyr
|
|
NM_001382787.1:c.3622G>T
|
NP_001369716.1:p.Asp1208Tyr
|
|
NM_001382788.1:c.3577G>T
|
NP_001369717.1:p.Asp1193Tyr
|
|
NM_001382789.1:c.3568G>T
|
NP_001369718.1:p.Asp1190Tyr
|
|
NM_001382790.1:c.3544G>T
|
NP_001369719.1:p.Asp1182Tyr
|
|
NM_001382791.1:c.3538G>T
|
NP_001369720.1:p.Asp1180Tyr
|
|
NM_001382792.1:c.3511G>T
|
NP_001369721.1:p.Asp1171Tyr
|
|
NM_001382793.1:c.3505G>T
|
NP_001369722.1:p.Asp1169Tyr
|
|
NM_001382794.1:c.3505G>T
|
NP_001369723.1:p.Asp1169Tyr
|
|
NM_001382795.1:c.3499G>T
|
NP_001369724.1:p.Asp1167Tyr
|
|
NM_001382796.1:c.3460G>T
|
NP_001369725.1:p.Asp1154Tyr
|
|
NM_001382797.1:c.3448G>T
|
NP_001369726.1:p.Asp1150Tyr
|
|
NM_001382798.1:c.3391G>T
|
NP_001369727.1:p.Asp1131Tyr
|
|
NM_001382799.1:c.3367G>T
|
NP_001369728.1:p.Asp1123Tyr
|
|
NM_001382800.1:c.3361G>T
|
NP_001369729.1:p.Asp1121Tyr
|
|
NM_001382801.1:c.3343G>T
|
NP_001369730.1:p.Asp1115Tyr
|
|
NM_001382802.1:c.3289G>T
|
NP_001369731.1:p.Asp1097Tyr
|
|
NM_001382803.1:c.*126G>T
|
NP_001369732.1:n.*126G>T
|
|
NM_001382804.1:c.2719G>T
|
NP_001369733.1:p.Asp907Tyr
|
|
NM_001382805.1:c.2596G>T
|
NP_001369734.1:p.Asp866Tyr
|
|
NM_001382806.1:c.2509G>T
|
NP_001369735.1:p.Asp837Tyr
|
|
NM_004448.4:c.3547G>T
MANE Select
|
NP_004439.2:p.Asp1183Tyr
|
|
NR_110535.2:n.3785G>T
|
|
|