ENST00000269571.10:c.3481C>T
MANE Select
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ENSP00000269571.4:p.Arg1161Ter
|
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ENST00000269571.9:c.3481C>T
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ENSP00000269571.4:p.Arg1161Ter
|
|
ENST00000406381.6:c.3391C>T
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ENSP00000385185.2:p.Arg1131Ter
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ENST00000445658.6:c.2653C>T
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ENSP00000404047.2:p.Arg885Ter
|
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ENST00000541774.5:c.3436C>T
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ENSP00000446466.1:p.Arg1146Ter
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ENST00000578373.5:c.*3271C>T
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ENSP00000463427.1:n.*3271C>T
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ENST00000584450.5:c.*60C>T
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ENSP00000463714.1:n.*60C>T
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ENST00000584601.5:c.3391C>T
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ENSP00000462438.1:p.Arg1131Ter
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NM_001005862.2:c.3391C>T , LRG_724t1:c.3391C>T
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NP_001005862.1:p.Arg1131Ter
|
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NM_001289936.1:c.3436C>T , LRG_724t4:c.3436C>T
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NP_001276865.1:p.Arg1146Ter
|
|
NM_001289937.1:c.*60C>T
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NP_001276866.1:n.*60C>T
|
|
NM_004448.3:c.3481C>T , LRG_724t2:c.3481C>T
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NP_004439.2:p.Arg1161Ter
|
|
NR_110535.1:n.3805C>T
|
|
|
XM_024450641.1:c.3619C>T
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XP_024306409.1:p.Arg1207Ter
|
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XM_024450642.1:c.3574C>T
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XP_024306410.1:p.Arg1192Ter
|
|
XM_024450643.1:c.3529C>T
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XP_024306411.1:p.Arg1177Ter
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NM_001005862.3:c.3391C>T
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NP_001005862.1:p.Arg1131Ter
|
|
NM_001289936.2:c.3436C>T
|
NP_001276865.1:p.Arg1146Ter
|
|
NM_001289937.2:c.*60C>T
|
NP_001276866.1:n.*60C>T
|
|
NM_001382782.1:c.3391C>T
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NP_001369711.1:p.Arg1131Ter
|
|
NM_001382783.1:c.3391C>T
|
NP_001369712.1:p.Arg1131Ter
|
|
NM_001382784.1:c.3598C>T
|
NP_001369713.1:p.Arg1200Ter
|
|
NM_001382785.1:c.3583C>T
|
NP_001369714.1:p.Arg1195Ter
|
|
NM_001382786.1:c.3562C>T
|
NP_001369715.1:p.Arg1188Ter
|
|
NM_001382787.1:c.3556C>T
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NP_001369716.1:p.Arg1186Ter
|
|
NM_001382788.1:c.3511C>T
|
NP_001369717.1:p.Arg1171Ter
|
|
NM_001382789.1:c.3502C>T
|
NP_001369718.1:p.Arg1168Ter
|
|
NM_001382790.1:c.3478C>T
|
NP_001369719.1:p.Arg1160Ter
|
|
NM_001382791.1:c.3472C>T
|
NP_001369720.1:p.Arg1158Ter
|
|
NM_001382792.1:c.3445C>T
|
NP_001369721.1:p.Arg1149Ter
|
|
NM_001382793.1:c.3439C>T
|
NP_001369722.1:p.Arg1147Ter
|
|
NM_001382794.1:c.3439C>T
|
NP_001369723.1:p.Arg1147Ter
|
|
NM_001382795.1:c.3433C>T
|
NP_001369724.1:p.Arg1145Ter
|
|
NM_001382796.1:c.3394C>T
|
NP_001369725.1:p.Arg1132Ter
|
|
NM_001382797.1:c.3382C>T
|
NP_001369726.1:p.Arg1128Ter
|
|
NM_001382798.1:c.3325C>T
|
NP_001369727.1:p.Arg1109Ter
|
|
NM_001382799.1:c.3301C>T
|
NP_001369728.1:p.Arg1101Ter
|
|
NM_001382800.1:c.3295C>T
|
NP_001369729.1:p.Arg1099Ter
|
|
NM_001382801.1:c.3277C>T
|
NP_001369730.1:p.Arg1093Ter
|
|
NM_001382802.1:c.3223C>T
|
NP_001369731.1:p.Arg1075Ter
|
|
NM_001382803.1:c.*60C>T
|
NP_001369732.1:n.*60C>T
|
|
NM_001382804.1:c.2653C>T
|
NP_001369733.1:p.Arg885Ter
|
|
NM_001382805.1:c.2530C>T
|
NP_001369734.1:p.Arg844Ter
|
|
NM_001382806.1:c.2443C>T
|
NP_001369735.1:p.Arg815Ter
|
|
NM_004448.4:c.3481C>T
MANE Select
|
NP_004439.2:p.Arg1161Ter
|
|
NR_110535.2:n.3719C>T
|
|
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