|
ENST00000269571.10:c.3667T>G
MANE Select
|
ENSP00000269571.4:p.Trp1223Gly
|
|
|
ENST00000269571.9:c.3667T>G
|
ENSP00000269571.4:p.Trp1223Gly
|
|
|
ENST00000406381.6:c.3577T>G
|
ENSP00000385185.2:p.Trp1193Gly
|
|
|
ENST00000445658.6:c.2839T>G
|
ENSP00000404047.2:p.Trp947Gly
|
|
|
ENST00000541774.5:c.3622T>G
|
ENSP00000446466.1:p.Trp1208Gly
|
|
|
ENST00000578373.5:c.*3457T>G
|
ENSP00000463427.1:n.*3457T>G
|
|
|
ENST00000584450.5:c.*246T>G
|
ENSP00000463714.1:n.*246T>G
|
|
|
ENST00000584601.5:c.3577T>G
|
ENSP00000462438.1:p.Trp1193Gly
|
|
|
NM_001005862.2:c.3577T>G , LRG_724t1:c.3577T>G
|
NP_001005862.1:p.Trp1193Gly
|
|
|
NM_001289936.1:c.3622T>G , LRG_724t4:c.3622T>G
|
NP_001276865.1:p.Trp1208Gly
|
|
|
NM_001289937.1:c.*246T>G
|
NP_001276866.1:n.*246T>G
|
|
|
NM_004448.3:c.3667T>G , LRG_724t2:c.3667T>G
|
NP_004439.2:p.Trp1223Gly
|
|
|
NR_110535.1:n.3991T>G
|
|
|
|
XM_024450641.1:c.3805T>G
|
XP_024306409.1:p.Trp1269Gly
|
|
|
XM_024450642.1:c.3760T>G
|
XP_024306410.1:p.Trp1254Gly
|
|
|
XM_024450643.1:c.3715T>G
|
XP_024306411.1:p.Trp1239Gly
|
|
|
NM_001005862.3:c.3577T>G
|
NP_001005862.1:p.Trp1193Gly
|
|
|
NM_001289936.2:c.3622T>G
|
NP_001276865.1:p.Trp1208Gly
|
|
|
NM_001289937.2:c.*246T>G
|
NP_001276866.1:n.*246T>G
|
|
|
NM_001382782.1:c.3577T>G
|
NP_001369711.1:p.Trp1193Gly
|
|
|
NM_001382783.1:c.3577T>G
|
NP_001369712.1:p.Trp1193Gly
|
|
|
NM_001382784.1:c.3784T>G
|
NP_001369713.1:p.Trp1262Gly
|
|
|
NM_001382785.1:c.3769T>G
|
NP_001369714.1:p.Trp1257Gly
|
|
|
NM_001382786.1:c.3748T>G
|
NP_001369715.1:p.Trp1250Gly
|
|
|
NM_001382787.1:c.3742T>G
|
NP_001369716.1:p.Trp1248Gly
|
|
|
NM_001382788.1:c.3697T>G
|
NP_001369717.1:p.Trp1233Gly
|
|
|
NM_001382789.1:c.3688T>G
|
NP_001369718.1:p.Trp1230Gly
|
|
|
NM_001382790.1:c.3664T>G
|
NP_001369719.1:p.Trp1222Gly
|
|
|
NM_001382791.1:c.3658T>G
|
NP_001369720.1:p.Trp1220Gly
|
|
|
NM_001382792.1:c.3631T>G
|
NP_001369721.1:p.Trp1211Gly
|
|
|
NM_001382793.1:c.3625T>G
|
NP_001369722.1:p.Trp1209Gly
|
|
|
NM_001382794.1:c.3625T>G
|
NP_001369723.1:p.Trp1209Gly
|
|
|
NM_001382795.1:c.3619T>G
|
NP_001369724.1:p.Trp1207Gly
|
|
|
NM_001382796.1:c.3580T>G
|
NP_001369725.1:p.Trp1194Gly
|
|
|
NM_001382797.1:c.3568T>G
|
NP_001369726.1:p.Trp1190Gly
|
|
|
NM_001382798.1:c.3511T>G
|
NP_001369727.1:p.Trp1171Gly
|
|
|
NM_001382799.1:c.3487T>G
|
NP_001369728.1:p.Trp1163Gly
|
|
|
NM_001382800.1:c.3481T>G
|
NP_001369729.1:p.Trp1161Gly
|
|
|
NM_001382801.1:c.3463T>G
|
NP_001369730.1:p.Trp1155Gly
|
|
|
NM_001382802.1:c.3409T>G
|
NP_001369731.1:p.Trp1137Gly
|
|
|
NM_001382803.1:c.*246T>G
|
NP_001369732.1:n.*246T>G
|
|
|
NM_001382804.1:c.2839T>G
|
NP_001369733.1:p.Trp947Gly
|
|
|
NM_001382805.1:c.2716T>G
|
NP_001369734.1:p.Trp906Gly
|
|
|
NM_001382806.1:c.2629T>G
|
NP_001369735.1:p.Trp877Gly
|
|
|
NM_004448.4:c.3667T>G
MANE Select
|
NP_004439.2:p.Trp1223Gly
|
|
|
NR_110535.2:n.3905T>G
|
|
|
