ENST00000269571.10:c.3652G>T
MANE Select
|
ENSP00000269571.4:p.Asp1218Tyr
|
|
ENST00000269571.9:c.3652G>T
|
ENSP00000269571.4:p.Asp1218Tyr
|
|
ENST00000406381.6:c.3562G>T
|
ENSP00000385185.2:p.Asp1188Tyr
|
|
ENST00000445658.6:c.2824G>T
|
ENSP00000404047.2:p.Asp942Tyr
|
|
ENST00000541774.5:c.3607G>T
|
ENSP00000446466.1:p.Asp1203Tyr
|
|
ENST00000578373.5:c.*3442G>T
|
ENSP00000463427.1:n.*3442G>T
|
|
ENST00000584450.5:c.*231G>T
|
ENSP00000463714.1:n.*231G>T
|
|
ENST00000584601.5:c.3562G>T
|
ENSP00000462438.1:p.Asp1188Tyr
|
|
NM_001005862.2:c.3562G>T , LRG_724t1:c.3562G>T
|
NP_001005862.1:p.Asp1188Tyr
|
|
NM_001289936.1:c.3607G>T , LRG_724t4:c.3607G>T
|
NP_001276865.1:p.Asp1203Tyr
|
|
NM_001289937.1:c.*231G>T
|
NP_001276866.1:n.*231G>T
|
|
NM_004448.3:c.3652G>T , LRG_724t2:c.3652G>T
|
NP_004439.2:p.Asp1218Tyr
|
|
NR_110535.1:n.3976G>T
|
|
|
XM_024450641.1:c.3790G>T
|
XP_024306409.1:p.Asp1264Tyr
|
|
XM_024450642.1:c.3745G>T
|
XP_024306410.1:p.Asp1249Tyr
|
|
XM_024450643.1:c.3700G>T
|
XP_024306411.1:p.Asp1234Tyr
|
|
NM_001005862.3:c.3562G>T
|
NP_001005862.1:p.Asp1188Tyr
|
|
NM_001289936.2:c.3607G>T
|
NP_001276865.1:p.Asp1203Tyr
|
|
NM_001289937.2:c.*231G>T
|
NP_001276866.1:n.*231G>T
|
|
NM_001382782.1:c.3562G>T
|
NP_001369711.1:p.Asp1188Tyr
|
|
NM_001382783.1:c.3562G>T
|
NP_001369712.1:p.Asp1188Tyr
|
|
NM_001382784.1:c.3769G>T
|
NP_001369713.1:p.Asp1257Tyr
|
|
NM_001382785.1:c.3754G>T
|
NP_001369714.1:p.Asp1252Tyr
|
|
NM_001382786.1:c.3733G>T
|
NP_001369715.1:p.Asp1245Tyr
|
|
NM_001382787.1:c.3727G>T
|
NP_001369716.1:p.Asp1243Tyr
|
|
NM_001382788.1:c.3682G>T
|
NP_001369717.1:p.Asp1228Tyr
|
|
NM_001382789.1:c.3673G>T
|
NP_001369718.1:p.Asp1225Tyr
|
|
NM_001382790.1:c.3649G>T
|
NP_001369719.1:p.Asp1217Tyr
|
|
NM_001382791.1:c.3643G>T
|
NP_001369720.1:p.Asp1215Tyr
|
|
NM_001382792.1:c.3616G>T
|
NP_001369721.1:p.Asp1206Tyr
|
|
NM_001382793.1:c.3610G>T
|
NP_001369722.1:p.Asp1204Tyr
|
|
NM_001382794.1:c.3610G>T
|
NP_001369723.1:p.Asp1204Tyr
|
|
NM_001382795.1:c.3604G>T
|
NP_001369724.1:p.Asp1202Tyr
|
|
NM_001382796.1:c.3565G>T
|
NP_001369725.1:p.Asp1189Tyr
|
|
NM_001382797.1:c.3553G>T
|
NP_001369726.1:p.Asp1185Tyr
|
|
NM_001382798.1:c.3496G>T
|
NP_001369727.1:p.Asp1166Tyr
|
|
NM_001382799.1:c.3472G>T
|
NP_001369728.1:p.Asp1158Tyr
|
|
NM_001382800.1:c.3466G>T
|
NP_001369729.1:p.Asp1156Tyr
|
|
NM_001382801.1:c.3448G>T
|
NP_001369730.1:p.Asp1150Tyr
|
|
NM_001382802.1:c.3394G>T
|
NP_001369731.1:p.Asp1132Tyr
|
|
NM_001382803.1:c.*231G>T
|
NP_001369732.1:n.*231G>T
|
|
NM_001382804.1:c.2824G>T
|
NP_001369733.1:p.Asp942Tyr
|
|
NM_001382805.1:c.2701G>T
|
NP_001369734.1:p.Asp901Tyr
|
|
NM_001382806.1:c.2614G>T
|
NP_001369735.1:p.Asp872Tyr
|
|
NM_004448.4:c.3652G>T
MANE Select
|
NP_004439.2:p.Asp1218Tyr
|
|
NR_110535.2:n.3890G>T
|
|
|