ENST00000269571.10:c.3438G>T
MANE Select
|
ENSP00000269571.4:p.Arg1146=
|
|
ENST00000269571.9:c.3438G>T
|
ENSP00000269571.4:p.Arg1146=
|
|
ENST00000406381.6:c.3348G>T
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ENSP00000385185.2:p.Arg1116=
|
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ENST00000445658.6:c.2610G>T
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ENSP00000404047.2:p.Arg870=
|
|
ENST00000541774.5:c.3393G>T
|
ENSP00000446466.1:p.Arg1131=
|
|
ENST00000578373.5:c.*3228G>T
|
ENSP00000463427.1:n.*3228G>T
|
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ENST00000584450.5:c.*17G>T
|
ENSP00000463714.1:n.*17G>T
|
|
ENST00000584601.5:c.3348G>T
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ENSP00000462438.1:p.Arg1116=
|
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NM_001005862.2:c.3348G>T , LRG_724t1:c.3348G>T
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NP_001005862.1:p.Arg1116=
|
|
NM_001289936.1:c.3393G>T , LRG_724t4:c.3393G>T
|
NP_001276865.1:p.Arg1131=
|
|
NM_001289937.1:c.*17G>T
|
NP_001276866.1:n.*17G>T
|
|
NM_004448.3:c.3438G>T , LRG_724t2:c.3438G>T
|
NP_004439.2:p.Arg1146=
|
|
NR_110535.1:n.3762G>T
|
|
|
XM_024450641.1:c.3576G>T
|
XP_024306409.1:p.Arg1192=
|
|
XM_024450642.1:c.3531G>T
|
XP_024306410.1:p.Arg1177=
|
|
XM_024450643.1:c.3486G>T
|
XP_024306411.1:p.Arg1162=
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|
NM_001005862.3:c.3348G>T
|
NP_001005862.1:p.Arg1116=
|
|
NM_001289936.2:c.3393G>T
|
NP_001276865.1:p.Arg1131=
|
|
NM_001289937.2:c.*17G>T
|
NP_001276866.1:n.*17G>T
|
|
NM_001382782.1:c.3348G>T
|
NP_001369711.1:p.Arg1116=
|
|
NM_001382783.1:c.3348G>T
|
NP_001369712.1:p.Arg1116=
|
|
NM_001382784.1:c.3555G>T
|
NP_001369713.1:p.Arg1185=
|
|
NM_001382785.1:c.3540G>T
|
NP_001369714.1:p.Arg1180=
|
|
NM_001382786.1:c.3519G>T
|
NP_001369715.1:p.Arg1173=
|
|
NM_001382787.1:c.3513G>T
|
NP_001369716.1:p.Arg1171=
|
|
NM_001382788.1:c.3468G>T
|
NP_001369717.1:p.Arg1156=
|
|
NM_001382789.1:c.3459G>T
|
NP_001369718.1:p.Arg1153=
|
|
NM_001382790.1:c.3435G>T
|
NP_001369719.1:p.Arg1145=
|
|
NM_001382791.1:c.3429G>T
|
NP_001369720.1:p.Arg1143=
|
|
NM_001382792.1:c.3402G>T
|
NP_001369721.1:p.Arg1134=
|
|
NM_001382793.1:c.3396G>T
|
NP_001369722.1:p.Arg1132=
|
|
NM_001382794.1:c.3396G>T
|
NP_001369723.1:p.Arg1132=
|
|
NM_001382795.1:c.3390G>T
|
NP_001369724.1:p.Arg1130=
|
|
NM_001382796.1:c.3351G>T
|
NP_001369725.1:p.Arg1117=
|
|
NM_001382797.1:c.3339G>T
|
NP_001369726.1:p.Arg1113=
|
|
NM_001382798.1:c.3282G>T
|
NP_001369727.1:p.Arg1094=
|
|
NM_001382799.1:c.3258G>T
|
NP_001369728.1:p.Arg1086=
|
|
NM_001382800.1:c.3252G>T
|
NP_001369729.1:p.Arg1084=
|
|
NM_001382801.1:c.3234G>T
|
NP_001369730.1:p.Arg1078=
|
|
NM_001382802.1:c.3180G>T
|
NP_001369731.1:p.Arg1060=
|
|
NM_001382803.1:c.*17G>T
|
NP_001369732.1:n.*17G>T
|
|
NM_001382804.1:c.2610G>T
|
NP_001369733.1:p.Arg870=
|
|
NM_001382805.1:c.2487G>T
|
NP_001369734.1:p.Arg829=
|
|
NM_001382806.1:c.2400G>T
|
NP_001369735.1:p.Arg800=
|
|
NM_004448.4:c.3438G>T
MANE Select
|
NP_004439.2:p.Arg1146=
|
|
NR_110535.2:n.3676G>T
|
|
|