ENST00000269571.10:c.3265G>C
MANE Select
|
ENSP00000269571.4:p.Asp1089His
|
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ENST00000269571.9:c.3265G>C
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ENSP00000269571.4:p.Asp1089His
|
|
ENST00000406381.6:c.3175G>C
|
ENSP00000385185.2:p.Asp1059His
|
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ENST00000445658.6:c.2437G>C
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ENSP00000404047.2:p.Asp813His
|
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ENST00000541774.5:c.3220G>C
|
ENSP00000446466.1:p.Asp1074His
|
|
ENST00000578373.5:c.*3055G>C
|
ENSP00000463427.1:n.*3055G>C
|
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ENST00000584450.5:c.3160-289G>C
|
ENSP00000463714.1:n.3160-289G>C
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ENST00000584601.5:c.3175G>C
|
ENSP00000462438.1:p.Asp1059His
|
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NM_001005862.2:c.3175G>C , LRG_724t1:c.3175G>C
|
NP_001005862.1:p.Asp1059His
|
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NM_001289936.1:c.3220G>C , LRG_724t4:c.3220G>C
|
NP_001276865.1:p.Asp1074His
|
|
NM_001289937.1:c.3160-289G>C
|
NP_001276866.1:n.3160-289G>C
|
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NM_004448.3:c.3265G>C , LRG_724t2:c.3265G>C
|
NP_004439.2:p.Asp1089His
|
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NR_110535.1:n.3589G>C
|
|
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XM_024450641.1:c.3403G>C
|
XP_024306409.1:p.Asp1135His
|
|
XM_024450642.1:c.3358G>C
|
XP_024306410.1:p.Asp1120His
|
|
XM_024450643.1:c.3313G>C
|
XP_024306411.1:p.Asp1105His
|
|
NM_001005862.3:c.3175G>C
|
NP_001005862.1:p.Asp1059His
|
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NM_001289936.2:c.3220G>C
|
NP_001276865.1:p.Asp1074His
|
|
NM_001289937.2:c.3160-289G>C
|
NP_001276866.1:n.3160-289G>C
|
|
NM_001382782.1:c.3175G>C
|
NP_001369711.1:p.Asp1059His
|
|
NM_001382783.1:c.3175G>C
|
NP_001369712.1:p.Asp1059His
|
|
NM_001382784.1:c.3382G>C
|
NP_001369713.1:p.Asp1128His
|
|
NM_001382785.1:c.3367G>C
|
NP_001369714.1:p.Asp1123His
|
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NM_001382786.1:c.3346G>C
|
NP_001369715.1:p.Asp1116His
|
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NM_001382787.1:c.3340G>C
|
NP_001369716.1:p.Asp1114His
|
|
NM_001382788.1:c.3295G>C
|
NP_001369717.1:p.Asp1099His
|
|
NM_001382789.1:c.3286G>C
|
NP_001369718.1:p.Asp1096His
|
|
NM_001382790.1:c.3262G>C
|
NP_001369719.1:p.Asp1088His
|
|
NM_001382791.1:c.3256G>C
|
NP_001369720.1:p.Asp1086His
|
|
NM_001382792.1:c.3229G>C
|
NP_001369721.1:p.Asp1077His
|
|
NM_001382793.1:c.3223G>C
|
NP_001369722.1:p.Asp1075His
|
|
NM_001382794.1:c.3223G>C
|
NP_001369723.1:p.Asp1075His
|
|
NM_001382795.1:c.3217G>C
|
NP_001369724.1:p.Asp1073His
|
|
NM_001382796.1:c.3178G>C
|
NP_001369725.1:p.Asp1060His
|
|
NM_001382797.1:c.3166G>C
|
NP_001369726.1:p.Asp1056His
|
|
NM_001382798.1:c.3109G>C
|
NP_001369727.1:p.Asp1037His
|
|
NM_001382799.1:c.3085G>C
|
NP_001369728.1:p.Asp1029His
|
|
NM_001382800.1:c.3079G>C
|
NP_001369729.1:p.Asp1027His
|
|
NM_001382801.1:c.3061G>C
|
NP_001369730.1:p.Asp1021His
|
|
NM_001382802.1:c.3007G>C
|
NP_001369731.1:p.Asp1003His
|
|
NM_001382803.1:c.3118-289G>C
|
NP_001369732.1:n.3118-289G>C
|
|
NM_001382804.1:c.2437G>C
|
NP_001369733.1:p.Asp813His
|
|
NM_001382805.1:c.2314G>C
|
NP_001369734.1:p.Asp772His
|
|
NM_001382806.1:c.2227G>C
|
NP_001369735.1:p.Asp743His
|
|
NM_004448.4:c.3265G>C
MANE Select
|
NP_004439.2:p.Asp1089His
|
|
NR_110535.2:n.3503G>C
|
|
|