|
ENST00000269571.10:c.3326T>G
MANE Select
|
ENSP00000269571.4:p.Leu1109Arg
|
|
|
ENST00000269571.9:c.3326T>G
|
ENSP00000269571.4:p.Leu1109Arg
|
|
|
ENST00000406381.6:c.3236T>G
|
ENSP00000385185.2:p.Leu1079Arg
|
|
|
ENST00000445658.6:c.2498T>G
|
ENSP00000404047.2:p.Leu833Arg
|
|
|
ENST00000541774.5:c.3281T>G
|
ENSP00000446466.1:p.Leu1094Arg
|
|
|
ENST00000578373.5:c.*3116T>G
|
ENSP00000463427.1:n.*3116T>G
|
|
|
ENST00000584450.5:c.3160-228T>G
|
ENSP00000463714.1:n.3160-228T>G
|
|
|
ENST00000584601.5:c.3236T>G
|
ENSP00000462438.1:p.Leu1079Arg
|
|
|
NM_001005862.2:c.3236T>G , LRG_724t1:c.3236T>G
|
NP_001005862.1:p.Leu1079Arg
|
|
|
NM_001289936.1:c.3281T>G , LRG_724t4:c.3281T>G
|
NP_001276865.1:p.Leu1094Arg
|
|
|
NM_001289937.1:c.3160-228T>G
|
NP_001276866.1:n.3160-228T>G
|
|
|
NM_004448.3:c.3326T>G , LRG_724t2:c.3326T>G
|
NP_004439.2:p.Leu1109Arg
|
|
|
NR_110535.1:n.3650T>G
|
|
|
|
XM_024450641.1:c.3464T>G
|
XP_024306409.1:p.Leu1155Arg
|
|
|
XM_024450642.1:c.3419T>G
|
XP_024306410.1:p.Leu1140Arg
|
|
|
XM_024450643.1:c.3374T>G
|
XP_024306411.1:p.Leu1125Arg
|
|
|
NM_001005862.3:c.3236T>G
|
NP_001005862.1:p.Leu1079Arg
|
|
|
NM_001289936.2:c.3281T>G
|
NP_001276865.1:p.Leu1094Arg
|
|
|
NM_001289937.2:c.3160-228T>G
|
NP_001276866.1:n.3160-228T>G
|
|
|
NM_001382782.1:c.3236T>G
|
NP_001369711.1:p.Leu1079Arg
|
|
|
NM_001382783.1:c.3236T>G
|
NP_001369712.1:p.Leu1079Arg
|
|
|
NM_001382784.1:c.3443T>G
|
NP_001369713.1:p.Leu1148Arg
|
|
|
NM_001382785.1:c.3428T>G
|
NP_001369714.1:p.Leu1143Arg
|
|
|
NM_001382786.1:c.3407T>G
|
NP_001369715.1:p.Leu1136Arg
|
|
|
NM_001382787.1:c.3401T>G
|
NP_001369716.1:p.Leu1134Arg
|
|
|
NM_001382788.1:c.3356T>G
|
NP_001369717.1:p.Leu1119Arg
|
|
|
NM_001382789.1:c.3347T>G
|
NP_001369718.1:p.Leu1116Arg
|
|
|
NM_001382790.1:c.3323T>G
|
NP_001369719.1:p.Leu1108Arg
|
|
|
NM_001382791.1:c.3317T>G
|
NP_001369720.1:p.Leu1106Arg
|
|
|
NM_001382792.1:c.3290T>G
|
NP_001369721.1:p.Leu1097Arg
|
|
|
NM_001382793.1:c.3284T>G
|
NP_001369722.1:p.Leu1095Arg
|
|
|
NM_001382794.1:c.3284T>G
|
NP_001369723.1:p.Leu1095Arg
|
|
|
NM_001382795.1:c.3278T>G
|
NP_001369724.1:p.Leu1093Arg
|
|
|
NM_001382796.1:c.3239T>G
|
NP_001369725.1:p.Leu1080Arg
|
|
|
NM_001382797.1:c.3227T>G
|
NP_001369726.1:p.Leu1076Arg
|
|
|
NM_001382798.1:c.3170T>G
|
NP_001369727.1:p.Leu1057Arg
|
|
|
NM_001382799.1:c.3146T>G
|
NP_001369728.1:p.Leu1049Arg
|
|
|
NM_001382800.1:c.3140T>G
|
NP_001369729.1:p.Leu1047Arg
|
|
|
NM_001382801.1:c.3122T>G
|
NP_001369730.1:p.Leu1041Arg
|
|
|
NM_001382802.1:c.3068T>G
|
NP_001369731.1:p.Leu1023Arg
|
|
|
NM_001382803.1:c.3118-228T>G
|
NP_001369732.1:n.3118-228T>G
|
|
|
NM_001382804.1:c.2498T>G
|
NP_001369733.1:p.Leu833Arg
|
|
|
NM_001382805.1:c.2375T>G
|
NP_001369734.1:p.Leu792Arg
|
|
|
NM_001382806.1:c.2288T>G
|
NP_001369735.1:p.Leu763Arg
|
|
|
NM_004448.4:c.3326T>G
MANE Select
|
NP_004439.2:p.Leu1109Arg
|
|
|
NR_110535.2:n.3564T>G
|
|
|
