|
ENST00000269571.10:c.3188T>G
MANE Select
|
ENSP00000269571.4:p.Leu1063Arg
|
|
|
ENST00000269571.9:c.3188T>G
|
ENSP00000269571.4:p.Leu1063Arg
|
|
|
ENST00000406381.6:c.3098T>G
|
ENSP00000385185.2:p.Leu1033Arg
|
|
|
ENST00000445658.6:c.2360T>G
|
ENSP00000404047.2:p.Leu787Arg
|
|
|
ENST00000541774.5:c.3143T>G
|
ENSP00000446466.1:p.Leu1048Arg
|
|
|
ENST00000578373.5:c.*2978T>G
|
ENSP00000463427.1:n.*2978T>G
|
|
|
ENST00000584450.5:c.3159+320T>G
|
ENSP00000463714.1:n.3159+320T>G
|
|
|
ENST00000584601.5:c.3098T>G
|
ENSP00000462438.1:p.Leu1033Arg
|
|
|
NM_001005862.2:c.3098T>G , LRG_724t1:c.3098T>G
|
NP_001005862.1:p.Leu1033Arg
|
|
|
NM_001289936.1:c.3143T>G , LRG_724t4:c.3143T>G
|
NP_001276865.1:p.Leu1048Arg
|
|
|
NM_001289937.1:c.3159+320T>G
|
NP_001276866.1:n.3159+320T>G
|
|
|
NM_004448.3:c.3188T>G , LRG_724t2:c.3188T>G
|
NP_004439.2:p.Leu1063Arg
|
|
|
NR_110535.1:n.3512T>G
|
|
|
|
XM_024450641.1:c.3326T>G
|
XP_024306409.1:p.Leu1109Arg
|
|
|
XM_024450642.1:c.3281T>G
|
XP_024306410.1:p.Leu1094Arg
|
|
|
XM_024450643.1:c.3236T>G
|
XP_024306411.1:p.Leu1079Arg
|
|
|
NM_001005862.3:c.3098T>G
|
NP_001005862.1:p.Leu1033Arg
|
|
|
NM_001289936.2:c.3143T>G
|
NP_001276865.1:p.Leu1048Arg
|
|
|
NM_001289937.2:c.3159+320T>G
|
NP_001276866.1:n.3159+320T>G
|
|
|
NM_001382782.1:c.3098T>G
|
NP_001369711.1:p.Leu1033Arg
|
|
|
NM_001382783.1:c.3098T>G
|
NP_001369712.1:p.Leu1033Arg
|
|
|
NM_001382784.1:c.3305T>G
|
NP_001369713.1:p.Leu1102Arg
|
|
|
NM_001382785.1:c.3290T>G
|
NP_001369714.1:p.Leu1097Arg
|
|
|
NM_001382786.1:c.3269T>G
|
NP_001369715.1:p.Leu1090Arg
|
|
|
NM_001382787.1:c.3263T>G
|
NP_001369716.1:p.Leu1088Arg
|
|
|
NM_001382788.1:c.3218T>G
|
NP_001369717.1:p.Leu1073Arg
|
|
|
NM_001382789.1:c.3209T>G
|
NP_001369718.1:p.Leu1070Arg
|
|
|
NM_001382790.1:c.3185T>G
|
NP_001369719.1:p.Leu1062Arg
|
|
|
NM_001382791.1:c.3179T>G
|
NP_001369720.1:p.Leu1060Arg
|
|
|
NM_001382792.1:c.3152T>G
|
NP_001369721.1:p.Leu1051Arg
|
|
|
NM_001382793.1:c.3146T>G
|
NP_001369722.1:p.Leu1049Arg
|
|
|
NM_001382794.1:c.3146T>G
|
NP_001369723.1:p.Leu1049Arg
|
|
|
NM_001382795.1:c.3140T>G
|
NP_001369724.1:p.Leu1047Arg
|
|
|
NM_001382796.1:c.3101T>G
|
NP_001369725.1:p.Leu1034Arg
|
|
|
NM_001382797.1:c.3089T>G
|
NP_001369726.1:p.Leu1030Arg
|
|
|
NM_001382798.1:c.3032T>G
|
NP_001369727.1:p.Leu1011Arg
|
|
|
NM_001382799.1:c.3008T>G
|
NP_001369728.1:p.Leu1003Arg
|
|
|
NM_001382800.1:c.3002T>G
|
NP_001369729.1:p.Leu1001Arg
|
|
|
NM_001382801.1:c.2984T>G
|
NP_001369730.1:p.Leu995Arg
|
|
|
NM_001382802.1:c.2930T>G
|
NP_001369731.1:p.Leu977Arg
|
|
|
NM_001382803.1:c.3117+320T>G
|
NP_001369732.1:n.3117+320T>G
|
|
|
NM_001382804.1:c.2360T>G
|
NP_001369733.1:p.Leu787Arg
|
|
|
NM_001382805.1:c.2237T>G
|
NP_001369734.1:p.Leu746Arg
|
|
|
NM_001382806.1:c.2150T>G
|
NP_001369735.1:p.Leu717Arg
|
|
|
NM_004448.4:c.3188T>G
MANE Select
|
NP_004439.2:p.Leu1063Arg
|
|
|
NR_110535.2:n.3426T>G
|
|
|
