ENST00000269571.10:c.3237A>T
MANE Select
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ENSP00000269571.4:p.Glu1079Asp
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ENST00000269571.9:c.3237A>T
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ENSP00000269571.4:p.Glu1079Asp
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ENST00000406381.6:c.3147A>T
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ENSP00000385185.2:p.Glu1049Asp
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ENST00000445658.6:c.2409A>T
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ENSP00000404047.2:p.Glu803Asp
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ENST00000541774.5:c.3192A>T
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ENSP00000446466.1:p.Glu1064Asp
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ENST00000578373.5:c.*3027A>T
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ENSP00000463427.1:n.*3027A>T
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ENST00000584450.5:c.3160-317A>T
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ENSP00000463714.1:n.3160-317A>T
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ENST00000584601.5:c.3147A>T
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ENSP00000462438.1:p.Glu1049Asp
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NM_001005862.2:c.3147A>T , LRG_724t1:c.3147A>T
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NP_001005862.1:p.Glu1049Asp
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NM_001289936.1:c.3192A>T , LRG_724t4:c.3192A>T
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NP_001276865.1:p.Glu1064Asp
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NM_001289937.1:c.3160-317A>T
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NP_001276866.1:n.3160-317A>T
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NM_004448.3:c.3237A>T , LRG_724t2:c.3237A>T
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NP_004439.2:p.Glu1079Asp
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NR_110535.1:n.3561A>T
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XM_024450641.1:c.3375A>T
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XP_024306409.1:p.Glu1125Asp
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XM_024450642.1:c.3330A>T
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XP_024306410.1:p.Glu1110Asp
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XM_024450643.1:c.3285A>T
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XP_024306411.1:p.Glu1095Asp
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NM_001005862.3:c.3147A>T
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NP_001005862.1:p.Glu1049Asp
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NM_001289936.2:c.3192A>T
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NP_001276865.1:p.Glu1064Asp
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NM_001289937.2:c.3160-317A>T
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NP_001276866.1:n.3160-317A>T
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NM_001382782.1:c.3147A>T
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NP_001369711.1:p.Glu1049Asp
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NM_001382783.1:c.3147A>T
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NP_001369712.1:p.Glu1049Asp
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NM_001382784.1:c.3354A>T
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NP_001369713.1:p.Glu1118Asp
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NM_001382785.1:c.3339A>T
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NP_001369714.1:p.Glu1113Asp
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NM_001382786.1:c.3318A>T
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NP_001369715.1:p.Glu1106Asp
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NM_001382787.1:c.3312A>T
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NP_001369716.1:p.Glu1104Asp
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NM_001382788.1:c.3267A>T
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NP_001369717.1:p.Glu1089Asp
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NM_001382789.1:c.3258A>T
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NP_001369718.1:p.Glu1086Asp
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NM_001382790.1:c.3234A>T
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NP_001369719.1:p.Glu1078Asp
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NM_001382791.1:c.3228A>T
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NP_001369720.1:p.Glu1076Asp
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NM_001382792.1:c.3201A>T
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NP_001369721.1:p.Glu1067Asp
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NM_001382793.1:c.3195A>T
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NP_001369722.1:p.Glu1065Asp
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NM_001382794.1:c.3195A>T
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NP_001369723.1:p.Glu1065Asp
|
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NM_001382795.1:c.3189A>T
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NP_001369724.1:p.Glu1063Asp
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NM_001382796.1:c.3150A>T
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NP_001369725.1:p.Glu1050Asp
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NM_001382797.1:c.3138A>T
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NP_001369726.1:p.Glu1046Asp
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NM_001382798.1:c.3081A>T
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NP_001369727.1:p.Glu1027Asp
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NM_001382799.1:c.3057A>T
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NP_001369728.1:p.Glu1019Asp
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NM_001382800.1:c.3051A>T
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NP_001369729.1:p.Glu1017Asp
|
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NM_001382801.1:c.3033A>T
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NP_001369730.1:p.Glu1011Asp
|
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NM_001382802.1:c.2979A>T
|
NP_001369731.1:p.Glu993Asp
|
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NM_001382803.1:c.3118-317A>T
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NP_001369732.1:n.3118-317A>T
|
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NM_001382804.1:c.2409A>T
|
NP_001369733.1:p.Glu803Asp
|
|
NM_001382805.1:c.2286A>T
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NP_001369734.1:p.Glu762Asp
|
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NM_001382806.1:c.2199A>T
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NP_001369735.1:p.Glu733Asp
|
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NM_004448.4:c.3237A>T
MANE Select
|
NP_004439.2:p.Glu1079Asp
|
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NR_110535.2:n.3475A>T
|
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