ENST00000269571.10:c.3637T>G
MANE Select
|
ENSP00000269571.4:p.Phe1213Val
|
|
ENST00000269571.9:c.3637T>G
|
ENSP00000269571.4:p.Phe1213Val
|
|
ENST00000406381.6:c.3547T>G
|
ENSP00000385185.2:p.Phe1183Val
|
|
ENST00000445658.6:c.2809T>G
|
ENSP00000404047.2:p.Phe937Val
|
|
ENST00000541774.5:c.3592T>G
|
ENSP00000446466.1:p.Phe1198Val
|
|
ENST00000578373.5:c.*3427T>G
|
ENSP00000463427.1:n.*3427T>G
|
|
ENST00000584450.5:c.*216T>G
|
ENSP00000463714.1:n.*216T>G
|
|
ENST00000584601.5:c.3547T>G
|
ENSP00000462438.1:p.Phe1183Val
|
|
NM_001005862.2:c.3547T>G , LRG_724t1:c.3547T>G
|
NP_001005862.1:p.Phe1183Val
|
|
NM_001289936.1:c.3592T>G , LRG_724t4:c.3592T>G
|
NP_001276865.1:p.Phe1198Val
|
|
NM_001289937.1:c.*216T>G
|
NP_001276866.1:n.*216T>G
|
|
NM_004448.3:c.3637T>G , LRG_724t2:c.3637T>G
|
NP_004439.2:p.Phe1213Val
|
|
NR_110535.1:n.3961T>G
|
|
|
XM_024450641.1:c.3775T>G
|
XP_024306409.1:p.Phe1259Val
|
|
XM_024450642.1:c.3730T>G
|
XP_024306410.1:p.Phe1244Val
|
|
XM_024450643.1:c.3685T>G
|
XP_024306411.1:p.Phe1229Val
|
|
NM_001005862.3:c.3547T>G
|
NP_001005862.1:p.Phe1183Val
|
|
NM_001289936.2:c.3592T>G
|
NP_001276865.1:p.Phe1198Val
|
|
NM_001289937.2:c.*216T>G
|
NP_001276866.1:n.*216T>G
|
|
NM_001382782.1:c.3547T>G
|
NP_001369711.1:p.Phe1183Val
|
|
NM_001382783.1:c.3547T>G
|
NP_001369712.1:p.Phe1183Val
|
|
NM_001382784.1:c.3754T>G
|
NP_001369713.1:p.Phe1252Val
|
|
NM_001382785.1:c.3739T>G
|
NP_001369714.1:p.Phe1247Val
|
|
NM_001382786.1:c.3718T>G
|
NP_001369715.1:p.Phe1240Val
|
|
NM_001382787.1:c.3712T>G
|
NP_001369716.1:p.Phe1238Val
|
|
NM_001382788.1:c.3667T>G
|
NP_001369717.1:p.Phe1223Val
|
|
NM_001382789.1:c.3658T>G
|
NP_001369718.1:p.Phe1220Val
|
|
NM_001382790.1:c.3634T>G
|
NP_001369719.1:p.Phe1212Val
|
|
NM_001382791.1:c.3628T>G
|
NP_001369720.1:p.Phe1210Val
|
|
NM_001382792.1:c.3601T>G
|
NP_001369721.1:p.Phe1201Val
|
|
NM_001382793.1:c.3595T>G
|
NP_001369722.1:p.Phe1199Val
|
|
NM_001382794.1:c.3595T>G
|
NP_001369723.1:p.Phe1199Val
|
|
NM_001382795.1:c.3589T>G
|
NP_001369724.1:p.Phe1197Val
|
|
NM_001382796.1:c.3550T>G
|
NP_001369725.1:p.Phe1184Val
|
|
NM_001382797.1:c.3538T>G
|
NP_001369726.1:p.Phe1180Val
|
|
NM_001382798.1:c.3481T>G
|
NP_001369727.1:p.Phe1161Val
|
|
NM_001382799.1:c.3457T>G
|
NP_001369728.1:p.Phe1153Val
|
|
NM_001382800.1:c.3451T>G
|
NP_001369729.1:p.Phe1151Val
|
|
NM_001382801.1:c.3433T>G
|
NP_001369730.1:p.Phe1145Val
|
|
NM_001382802.1:c.3379T>G
|
NP_001369731.1:p.Phe1127Val
|
|
NM_001382803.1:c.*216T>G
|
NP_001369732.1:n.*216T>G
|
|
NM_001382804.1:c.2809T>G
|
NP_001369733.1:p.Phe937Val
|
|
NM_001382805.1:c.2686T>G
|
NP_001369734.1:p.Phe896Val
|
|
NM_001382806.1:c.2599T>G
|
NP_001369735.1:p.Phe867Val
|
|
NM_004448.4:c.3637T>G
MANE Select
|
NP_004439.2:p.Phe1213Val
|
|
NR_110535.2:n.3875T>G
|
|
|