ENST00000269571.10:c.3528G>T
MANE Select
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ENSP00000269571.4:p.Gly1176=
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ENST00000269571.9:c.3528G>T
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ENSP00000269571.4:p.Gly1176=
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ENST00000406381.6:c.3438G>T
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ENSP00000385185.2:p.Gly1146=
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ENST00000445658.6:c.2700G>T
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ENSP00000404047.2:p.Gly900=
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ENST00000541774.5:c.3483G>T
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ENSP00000446466.1:p.Gly1161=
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ENST00000578373.5:c.*3318G>T
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ENSP00000463427.1:n.*3318G>T
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ENST00000584450.5:c.*107G>T
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ENSP00000463714.1:n.*107G>T
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ENST00000584601.5:c.3438G>T
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ENSP00000462438.1:p.Gly1146=
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NM_001005862.2:c.3438G>T , LRG_724t1:c.3438G>T
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NP_001005862.1:p.Gly1146=
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NM_001289936.1:c.3483G>T , LRG_724t4:c.3483G>T
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NP_001276865.1:p.Gly1161=
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NM_001289937.1:c.*107G>T
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NP_001276866.1:n.*107G>T
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NM_004448.3:c.3528G>T , LRG_724t2:c.3528G>T
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NP_004439.2:p.Gly1176=
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NR_110535.1:n.3852G>T
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XM_024450641.1:c.3666G>T
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XP_024306409.1:p.Gly1222=
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XM_024450642.1:c.3621G>T
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XP_024306410.1:p.Gly1207=
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XM_024450643.1:c.3576G>T
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XP_024306411.1:p.Gly1192=
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NM_001005862.3:c.3438G>T
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NP_001005862.1:p.Gly1146=
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NM_001289936.2:c.3483G>T
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NP_001276865.1:p.Gly1161=
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NM_001289937.2:c.*107G>T
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NP_001276866.1:n.*107G>T
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NM_001382782.1:c.3438G>T
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NP_001369711.1:p.Gly1146=
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NM_001382783.1:c.3438G>T
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NP_001369712.1:p.Gly1146=
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NM_001382784.1:c.3645G>T
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NP_001369713.1:p.Gly1215=
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NM_001382785.1:c.3630G>T
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NP_001369714.1:p.Gly1210=
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NM_001382786.1:c.3609G>T
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NP_001369715.1:p.Gly1203=
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NM_001382787.1:c.3603G>T
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NP_001369716.1:p.Gly1201=
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NM_001382788.1:c.3558G>T
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NP_001369717.1:p.Gly1186=
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NM_001382789.1:c.3549G>T
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NP_001369718.1:p.Gly1183=
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NM_001382790.1:c.3525G>T
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NP_001369719.1:p.Gly1175=
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NM_001382791.1:c.3519G>T
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NP_001369720.1:p.Gly1173=
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NM_001382792.1:c.3492G>T
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NP_001369721.1:p.Gly1164=
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NM_001382793.1:c.3486G>T
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NP_001369722.1:p.Gly1162=
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NM_001382794.1:c.3486G>T
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NP_001369723.1:p.Gly1162=
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NM_001382795.1:c.3480G>T
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NP_001369724.1:p.Gly1160=
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NM_001382796.1:c.3441G>T
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NP_001369725.1:p.Gly1147=
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NM_001382797.1:c.3429G>T
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NP_001369726.1:p.Gly1143=
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NM_001382798.1:c.3372G>T
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NP_001369727.1:p.Gly1124=
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NM_001382799.1:c.3348G>T
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NP_001369728.1:p.Gly1116=
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NM_001382800.1:c.3342G>T
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NP_001369729.1:p.Gly1114=
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NM_001382801.1:c.3324G>T
|
NP_001369730.1:p.Gly1108=
|
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NM_001382802.1:c.3270G>T
|
NP_001369731.1:p.Gly1090=
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NM_001382803.1:c.*107G>T
|
NP_001369732.1:n.*107G>T
|
|
NM_001382804.1:c.2700G>T
|
NP_001369733.1:p.Gly900=
|
|
NM_001382805.1:c.2577G>T
|
NP_001369734.1:p.Gly859=
|
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NM_001382806.1:c.2490G>T
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NP_001369735.1:p.Gly830=
|
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NM_004448.4:c.3528G>T
MANE Select
|
NP_004439.2:p.Gly1176=
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NR_110535.2:n.3766G>T
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