ENST00000269571.10:c.3369G>T
MANE Select
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ENSP00000269571.4:p.Glu1123Asp
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ENST00000269571.9:c.3369G>T
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ENSP00000269571.4:p.Glu1123Asp
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ENST00000406381.6:c.3279G>T
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ENSP00000385185.2:p.Glu1093Asp
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ENST00000445658.6:c.2541G>T
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ENSP00000404047.2:p.Glu847Asp
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ENST00000541774.5:c.3324G>T
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ENSP00000446466.1:p.Glu1108Asp
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ENST00000578373.5:c.*3159G>T
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ENSP00000463427.1:n.*3159G>T
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ENST00000584450.5:c.3160-185G>T
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ENSP00000463714.1:n.3160-185G>T
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ENST00000584601.5:c.3279G>T
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ENSP00000462438.1:p.Glu1093Asp
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NM_001005862.2:c.3279G>T , LRG_724t1:c.3279G>T
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NP_001005862.1:p.Glu1093Asp
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NM_001289936.1:c.3324G>T , LRG_724t4:c.3324G>T
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NP_001276865.1:p.Glu1108Asp
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NM_001289937.1:c.3160-185G>T
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NP_001276866.1:n.3160-185G>T
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NM_004448.3:c.3369G>T , LRG_724t2:c.3369G>T
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NP_004439.2:p.Glu1123Asp
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NR_110535.1:n.3693G>T
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XM_024450641.1:c.3507G>T
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XP_024306409.1:p.Glu1169Asp
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XM_024450642.1:c.3462G>T
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XP_024306410.1:p.Glu1154Asp
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XM_024450643.1:c.3417G>T
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XP_024306411.1:p.Glu1139Asp
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NM_001005862.3:c.3279G>T
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NP_001005862.1:p.Glu1093Asp
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NM_001289936.2:c.3324G>T
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NP_001276865.1:p.Glu1108Asp
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NM_001289937.2:c.3160-185G>T
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NP_001276866.1:n.3160-185G>T
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NM_001382782.1:c.3279G>T
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NP_001369711.1:p.Glu1093Asp
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NM_001382783.1:c.3279G>T
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NP_001369712.1:p.Glu1093Asp
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|
NM_001382784.1:c.3486G>T
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NP_001369713.1:p.Glu1162Asp
|
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NM_001382785.1:c.3471G>T
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NP_001369714.1:p.Glu1157Asp
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NM_001382786.1:c.3450G>T
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NP_001369715.1:p.Glu1150Asp
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NM_001382787.1:c.3444G>T
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NP_001369716.1:p.Glu1148Asp
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NM_001382788.1:c.3399G>T
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NP_001369717.1:p.Glu1133Asp
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NM_001382789.1:c.3390G>T
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NP_001369718.1:p.Glu1130Asp
|
|
NM_001382790.1:c.3366G>T
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NP_001369719.1:p.Glu1122Asp
|
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NM_001382791.1:c.3360G>T
|
NP_001369720.1:p.Glu1120Asp
|
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NM_001382792.1:c.3333G>T
|
NP_001369721.1:p.Glu1111Asp
|
|
NM_001382793.1:c.3327G>T
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NP_001369722.1:p.Glu1109Asp
|
|
NM_001382794.1:c.3327G>T
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NP_001369723.1:p.Glu1109Asp
|
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NM_001382795.1:c.3321G>T
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NP_001369724.1:p.Glu1107Asp
|
|
NM_001382796.1:c.3282G>T
|
NP_001369725.1:p.Glu1094Asp
|
|
NM_001382797.1:c.3270G>T
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NP_001369726.1:p.Glu1090Asp
|
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NM_001382798.1:c.3213G>T
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NP_001369727.1:p.Glu1071Asp
|
|
NM_001382799.1:c.3189G>T
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NP_001369728.1:p.Glu1063Asp
|
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NM_001382800.1:c.3183G>T
|
NP_001369729.1:p.Glu1061Asp
|
|
NM_001382801.1:c.3165G>T
|
NP_001369730.1:p.Glu1055Asp
|
|
NM_001382802.1:c.3111G>T
|
NP_001369731.1:p.Glu1037Asp
|
|
NM_001382803.1:c.3118-185G>T
|
NP_001369732.1:n.3118-185G>T
|
|
NM_001382804.1:c.2541G>T
|
NP_001369733.1:p.Glu847Asp
|
|
NM_001382805.1:c.2418G>T
|
NP_001369734.1:p.Glu806Asp
|
|
NM_001382806.1:c.2331G>T
|
NP_001369735.1:p.Glu777Asp
|
|
NM_004448.4:c.3369G>T
MANE Select
|
NP_004439.2:p.Glu1123Asp
|
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NR_110535.2:n.3607G>T
|
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