ENST00000269571.10:c.3266A>T
MANE Select
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ENSP00000269571.4:p.Asp1089Val
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ENST00000269571.9:c.3266A>T
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ENSP00000269571.4:p.Asp1089Val
|
|
ENST00000406381.6:c.3176A>T
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ENSP00000385185.2:p.Asp1059Val
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ENST00000445658.6:c.2438A>T
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ENSP00000404047.2:p.Asp813Val
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ENST00000541774.5:c.3221A>T
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ENSP00000446466.1:p.Asp1074Val
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ENST00000578373.5:c.*3056A>T
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ENSP00000463427.1:n.*3056A>T
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ENST00000584450.5:c.3160-288A>T
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ENSP00000463714.1:n.3160-288A>T
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ENST00000584601.5:c.3176A>T
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ENSP00000462438.1:p.Asp1059Val
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NM_001005862.2:c.3176A>T , LRG_724t1:c.3176A>T
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NP_001005862.1:p.Asp1059Val
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NM_001289936.1:c.3221A>T , LRG_724t4:c.3221A>T
|
NP_001276865.1:p.Asp1074Val
|
|
NM_001289937.1:c.3160-288A>T
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NP_001276866.1:n.3160-288A>T
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NM_004448.3:c.3266A>T , LRG_724t2:c.3266A>T
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NP_004439.2:p.Asp1089Val
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NR_110535.1:n.3590A>T
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|
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XM_024450641.1:c.3404A>T
|
XP_024306409.1:p.Asp1135Val
|
|
XM_024450642.1:c.3359A>T
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XP_024306410.1:p.Asp1120Val
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|
XM_024450643.1:c.3314A>T
|
XP_024306411.1:p.Asp1105Val
|
|
NM_001005862.3:c.3176A>T
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NP_001005862.1:p.Asp1059Val
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NM_001289936.2:c.3221A>T
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NP_001276865.1:p.Asp1074Val
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|
NM_001289937.2:c.3160-288A>T
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NP_001276866.1:n.3160-288A>T
|
|
NM_001382782.1:c.3176A>T
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NP_001369711.1:p.Asp1059Val
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|
NM_001382783.1:c.3176A>T
|
NP_001369712.1:p.Asp1059Val
|
|
NM_001382784.1:c.3383A>T
|
NP_001369713.1:p.Asp1128Val
|
|
NM_001382785.1:c.3368A>T
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NP_001369714.1:p.Asp1123Val
|
|
NM_001382786.1:c.3347A>T
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NP_001369715.1:p.Asp1116Val
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NM_001382787.1:c.3341A>T
|
NP_001369716.1:p.Asp1114Val
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|
NM_001382788.1:c.3296A>T
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NP_001369717.1:p.Asp1099Val
|
|
NM_001382789.1:c.3287A>T
|
NP_001369718.1:p.Asp1096Val
|
|
NM_001382790.1:c.3263A>T
|
NP_001369719.1:p.Asp1088Val
|
|
NM_001382791.1:c.3257A>T
|
NP_001369720.1:p.Asp1086Val
|
|
NM_001382792.1:c.3230A>T
|
NP_001369721.1:p.Asp1077Val
|
|
NM_001382793.1:c.3224A>T
|
NP_001369722.1:p.Asp1075Val
|
|
NM_001382794.1:c.3224A>T
|
NP_001369723.1:p.Asp1075Val
|
|
NM_001382795.1:c.3218A>T
|
NP_001369724.1:p.Asp1073Val
|
|
NM_001382796.1:c.3179A>T
|
NP_001369725.1:p.Asp1060Val
|
|
NM_001382797.1:c.3167A>T
|
NP_001369726.1:p.Asp1056Val
|
|
NM_001382798.1:c.3110A>T
|
NP_001369727.1:p.Asp1037Val
|
|
NM_001382799.1:c.3086A>T
|
NP_001369728.1:p.Asp1029Val
|
|
NM_001382800.1:c.3080A>T
|
NP_001369729.1:p.Asp1027Val
|
|
NM_001382801.1:c.3062A>T
|
NP_001369730.1:p.Asp1021Val
|
|
NM_001382802.1:c.3008A>T
|
NP_001369731.1:p.Asp1003Val
|
|
NM_001382803.1:c.3118-288A>T
|
NP_001369732.1:n.3118-288A>T
|
|
NM_001382804.1:c.2438A>T
|
NP_001369733.1:p.Asp813Val
|
|
NM_001382805.1:c.2315A>T
|
NP_001369734.1:p.Asp772Val
|
|
NM_001382806.1:c.2228A>T
|
NP_001369735.1:p.Asp743Val
|
|
NM_004448.4:c.3266A>T
MANE Select
|
NP_004439.2:p.Asp1089Val
|
|
NR_110535.2:n.3504A>T
|
|
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