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ENST00000269571.10:c.3650T>G
MANE Select
|
ENSP00000269571.4:p.Phe1217Cys
|
|
|
ENST00000269571.9:c.3650T>G
|
ENSP00000269571.4:p.Phe1217Cys
|
|
|
ENST00000406381.6:c.3560T>G
|
ENSP00000385185.2:p.Phe1187Cys
|
|
|
ENST00000445658.6:c.2822T>G
|
ENSP00000404047.2:p.Phe941Cys
|
|
|
ENST00000541774.5:c.3605T>G
|
ENSP00000446466.1:p.Phe1202Cys
|
|
|
ENST00000578373.5:c.*3440T>G
|
ENSP00000463427.1:n.*3440T>G
|
|
|
ENST00000584450.5:c.*229T>G
|
ENSP00000463714.1:n.*229T>G
|
|
|
ENST00000584601.5:c.3560T>G
|
ENSP00000462438.1:p.Phe1187Cys
|
|
|
NM_001005862.2:c.3560T>G , LRG_724t1:c.3560T>G
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NP_001005862.1:p.Phe1187Cys
|
|
|
NM_001289936.1:c.3605T>G , LRG_724t4:c.3605T>G
|
NP_001276865.1:p.Phe1202Cys
|
|
|
NM_001289937.1:c.*229T>G
|
NP_001276866.1:n.*229T>G
|
|
|
NM_004448.3:c.3650T>G , LRG_724t2:c.3650T>G
|
NP_004439.2:p.Phe1217Cys
|
|
|
NR_110535.1:n.3974T>G
|
|
|
|
XM_024450641.1:c.3788T>G
|
XP_024306409.1:p.Phe1263Cys
|
|
|
XM_024450642.1:c.3743T>G
|
XP_024306410.1:p.Phe1248Cys
|
|
|
XM_024450643.1:c.3698T>G
|
XP_024306411.1:p.Phe1233Cys
|
|
|
NM_001005862.3:c.3560T>G
|
NP_001005862.1:p.Phe1187Cys
|
|
|
NM_001289936.2:c.3605T>G
|
NP_001276865.1:p.Phe1202Cys
|
|
|
NM_001289937.2:c.*229T>G
|
NP_001276866.1:n.*229T>G
|
|
|
NM_001382782.1:c.3560T>G
|
NP_001369711.1:p.Phe1187Cys
|
|
|
NM_001382783.1:c.3560T>G
|
NP_001369712.1:p.Phe1187Cys
|
|
|
NM_001382784.1:c.3767T>G
|
NP_001369713.1:p.Phe1256Cys
|
|
|
NM_001382785.1:c.3752T>G
|
NP_001369714.1:p.Phe1251Cys
|
|
|
NM_001382786.1:c.3731T>G
|
NP_001369715.1:p.Phe1244Cys
|
|
|
NM_001382787.1:c.3725T>G
|
NP_001369716.1:p.Phe1242Cys
|
|
|
NM_001382788.1:c.3680T>G
|
NP_001369717.1:p.Phe1227Cys
|
|
|
NM_001382789.1:c.3671T>G
|
NP_001369718.1:p.Phe1224Cys
|
|
|
NM_001382790.1:c.3647T>G
|
NP_001369719.1:p.Phe1216Cys
|
|
|
NM_001382791.1:c.3641T>G
|
NP_001369720.1:p.Phe1214Cys
|
|
|
NM_001382792.1:c.3614T>G
|
NP_001369721.1:p.Phe1205Cys
|
|
|
NM_001382793.1:c.3608T>G
|
NP_001369722.1:p.Phe1203Cys
|
|
|
NM_001382794.1:c.3608T>G
|
NP_001369723.1:p.Phe1203Cys
|
|
|
NM_001382795.1:c.3602T>G
|
NP_001369724.1:p.Phe1201Cys
|
|
|
NM_001382796.1:c.3563T>G
|
NP_001369725.1:p.Phe1188Cys
|
|
|
NM_001382797.1:c.3551T>G
|
NP_001369726.1:p.Phe1184Cys
|
|
|
NM_001382798.1:c.3494T>G
|
NP_001369727.1:p.Phe1165Cys
|
|
|
NM_001382799.1:c.3470T>G
|
NP_001369728.1:p.Phe1157Cys
|
|
|
NM_001382800.1:c.3464T>G
|
NP_001369729.1:p.Phe1155Cys
|
|
|
NM_001382801.1:c.3446T>G
|
NP_001369730.1:p.Phe1149Cys
|
|
|
NM_001382802.1:c.3392T>G
|
NP_001369731.1:p.Phe1131Cys
|
|
|
NM_001382803.1:c.*229T>G
|
NP_001369732.1:n.*229T>G
|
|
|
NM_001382804.1:c.2822T>G
|
NP_001369733.1:p.Phe941Cys
|
|
|
NM_001382805.1:c.2699T>G
|
NP_001369734.1:p.Phe900Cys
|
|
|
NM_001382806.1:c.2612T>G
|
NP_001369735.1:p.Phe871Cys
|
|
|
NM_004448.4:c.3650T>G
MANE Select
|
NP_004439.2:p.Phe1217Cys
|
|
|
NR_110535.2:n.3888T>G
|
|
|
