ENST00000269571.10:c.3313G>T
MANE Select
|
ENSP00000269571.4:p.Asp1105Tyr
|
|
ENST00000269571.9:c.3313G>T
|
ENSP00000269571.4:p.Asp1105Tyr
|
|
ENST00000406381.6:c.3223G>T
|
ENSP00000385185.2:p.Asp1075Tyr
|
|
ENST00000445658.6:c.2485G>T
|
ENSP00000404047.2:p.Asp829Tyr
|
|
ENST00000541774.5:c.3268G>T
|
ENSP00000446466.1:p.Asp1090Tyr
|
|
ENST00000578373.5:c.*3103G>T
|
ENSP00000463427.1:n.*3103G>T
|
|
ENST00000584450.5:c.3160-241G>T
|
ENSP00000463714.1:n.3160-241G>T
|
|
ENST00000584601.5:c.3223G>T
|
ENSP00000462438.1:p.Asp1075Tyr
|
|
NM_001005862.2:c.3223G>T , LRG_724t1:c.3223G>T
|
NP_001005862.1:p.Asp1075Tyr
|
|
NM_001289936.1:c.3268G>T , LRG_724t4:c.3268G>T
|
NP_001276865.1:p.Asp1090Tyr
|
|
NM_001289937.1:c.3160-241G>T
|
NP_001276866.1:n.3160-241G>T
|
|
NM_004448.3:c.3313G>T , LRG_724t2:c.3313G>T
|
NP_004439.2:p.Asp1105Tyr
|
|
NR_110535.1:n.3637G>T
|
|
|
XM_024450641.1:c.3451G>T
|
XP_024306409.1:p.Asp1151Tyr
|
|
XM_024450642.1:c.3406G>T
|
XP_024306410.1:p.Asp1136Tyr
|
|
XM_024450643.1:c.3361G>T
|
XP_024306411.1:p.Asp1121Tyr
|
|
NM_001005862.3:c.3223G>T
|
NP_001005862.1:p.Asp1075Tyr
|
|
NM_001289936.2:c.3268G>T
|
NP_001276865.1:p.Asp1090Tyr
|
|
NM_001289937.2:c.3160-241G>T
|
NP_001276866.1:n.3160-241G>T
|
|
NM_001382782.1:c.3223G>T
|
NP_001369711.1:p.Asp1075Tyr
|
|
NM_001382783.1:c.3223G>T
|
NP_001369712.1:p.Asp1075Tyr
|
|
NM_001382784.1:c.3430G>T
|
NP_001369713.1:p.Asp1144Tyr
|
|
NM_001382785.1:c.3415G>T
|
NP_001369714.1:p.Asp1139Tyr
|
|
NM_001382786.1:c.3394G>T
|
NP_001369715.1:p.Asp1132Tyr
|
|
NM_001382787.1:c.3388G>T
|
NP_001369716.1:p.Asp1130Tyr
|
|
NM_001382788.1:c.3343G>T
|
NP_001369717.1:p.Asp1115Tyr
|
|
NM_001382789.1:c.3334G>T
|
NP_001369718.1:p.Asp1112Tyr
|
|
NM_001382790.1:c.3310G>T
|
NP_001369719.1:p.Asp1104Tyr
|
|
NM_001382791.1:c.3304G>T
|
NP_001369720.1:p.Asp1102Tyr
|
|
NM_001382792.1:c.3277G>T
|
NP_001369721.1:p.Asp1093Tyr
|
|
NM_001382793.1:c.3271G>T
|
NP_001369722.1:p.Asp1091Tyr
|
|
NM_001382794.1:c.3271G>T
|
NP_001369723.1:p.Asp1091Tyr
|
|
NM_001382795.1:c.3265G>T
|
NP_001369724.1:p.Asp1089Tyr
|
|
NM_001382796.1:c.3226G>T
|
NP_001369725.1:p.Asp1076Tyr
|
|
NM_001382797.1:c.3214G>T
|
NP_001369726.1:p.Asp1072Tyr
|
|
NM_001382798.1:c.3157G>T
|
NP_001369727.1:p.Asp1053Tyr
|
|
NM_001382799.1:c.3133G>T
|
NP_001369728.1:p.Asp1045Tyr
|
|
NM_001382800.1:c.3127G>T
|
NP_001369729.1:p.Asp1043Tyr
|
|
NM_001382801.1:c.3109G>T
|
NP_001369730.1:p.Asp1037Tyr
|
|
NM_001382802.1:c.3055G>T
|
NP_001369731.1:p.Asp1019Tyr
|
|
NM_001382803.1:c.3118-241G>T
|
NP_001369732.1:n.3118-241G>T
|
|
NM_001382804.1:c.2485G>T
|
NP_001369733.1:p.Asp829Tyr
|
|
NM_001382805.1:c.2362G>T
|
NP_001369734.1:p.Asp788Tyr
|
|
NM_001382806.1:c.2275G>T
|
NP_001369735.1:p.Asp759Tyr
|
|
NM_004448.4:c.3313G>T
MANE Select
|
NP_004439.2:p.Asp1105Tyr
|
|
NR_110535.2:n.3551G>T
|
|
|