ENST00000269571.10:c.3204G>T
MANE Select
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ENSP00000269571.4:p.Glu1068Asp
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ENST00000269571.9:c.3204G>T
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ENSP00000269571.4:p.Glu1068Asp
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ENST00000406381.6:c.3114G>T
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ENSP00000385185.2:p.Glu1038Asp
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ENST00000445658.6:c.2376G>T
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ENSP00000404047.2:p.Glu792Asp
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ENST00000541774.5:c.3159G>T
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ENSP00000446466.1:p.Glu1053Asp
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ENST00000578373.5:c.*2994G>T
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ENSP00000463427.1:n.*2994G>T
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ENST00000584450.5:c.3159+336G>T
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ENSP00000463714.1:n.3159+336G>T
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ENST00000584601.5:c.3114G>T
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ENSP00000462438.1:p.Glu1038Asp
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NM_001005862.2:c.3114G>T , LRG_724t1:c.3114G>T
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NP_001005862.1:p.Glu1038Asp
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NM_001289936.1:c.3159G>T , LRG_724t4:c.3159G>T
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NP_001276865.1:p.Glu1053Asp
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NM_001289937.1:c.3159+336G>T
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NP_001276866.1:n.3159+336G>T
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NM_004448.3:c.3204G>T , LRG_724t2:c.3204G>T
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NP_004439.2:p.Glu1068Asp
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NR_110535.1:n.3528G>T
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|
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XM_024450641.1:c.3342G>T
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XP_024306409.1:p.Glu1114Asp
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XM_024450642.1:c.3297G>T
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XP_024306410.1:p.Glu1099Asp
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XM_024450643.1:c.3252G>T
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XP_024306411.1:p.Glu1084Asp
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NM_001005862.3:c.3114G>T
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NP_001005862.1:p.Glu1038Asp
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NM_001289936.2:c.3159G>T
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NP_001276865.1:p.Glu1053Asp
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NM_001289937.2:c.3159+336G>T
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NP_001276866.1:n.3159+336G>T
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NM_001382782.1:c.3114G>T
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NP_001369711.1:p.Glu1038Asp
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NM_001382783.1:c.3114G>T
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NP_001369712.1:p.Glu1038Asp
|
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NM_001382784.1:c.3321G>T
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NP_001369713.1:p.Glu1107Asp
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NM_001382785.1:c.3306G>T
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NP_001369714.1:p.Glu1102Asp
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NM_001382786.1:c.3285G>T
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NP_001369715.1:p.Glu1095Asp
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NM_001382787.1:c.3279G>T
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NP_001369716.1:p.Glu1093Asp
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NM_001382788.1:c.3234G>T
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NP_001369717.1:p.Glu1078Asp
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NM_001382789.1:c.3225G>T
|
NP_001369718.1:p.Glu1075Asp
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NM_001382790.1:c.3201G>T
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NP_001369719.1:p.Glu1067Asp
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|
NM_001382791.1:c.3195G>T
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NP_001369720.1:p.Glu1065Asp
|
|
NM_001382792.1:c.3168G>T
|
NP_001369721.1:p.Glu1056Asp
|
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NM_001382793.1:c.3162G>T
|
NP_001369722.1:p.Glu1054Asp
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NM_001382794.1:c.3162G>T
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NP_001369723.1:p.Glu1054Asp
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|
NM_001382795.1:c.3156G>T
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NP_001369724.1:p.Glu1052Asp
|
|
NM_001382796.1:c.3117G>T
|
NP_001369725.1:p.Glu1039Asp
|
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NM_001382797.1:c.3105G>T
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NP_001369726.1:p.Glu1035Asp
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|
NM_001382798.1:c.3048G>T
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NP_001369727.1:p.Glu1016Asp
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NM_001382799.1:c.3024G>T
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NP_001369728.1:p.Glu1008Asp
|
|
NM_001382800.1:c.3018G>T
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NP_001369729.1:p.Glu1006Asp
|
|
NM_001382801.1:c.3000G>T
|
NP_001369730.1:p.Glu1000Asp
|
|
NM_001382802.1:c.2946G>T
|
NP_001369731.1:p.Glu982Asp
|
|
NM_001382803.1:c.3117+336G>T
|
NP_001369732.1:n.3117+336G>T
|
|
NM_001382804.1:c.2376G>T
|
NP_001369733.1:p.Glu792Asp
|
|
NM_001382805.1:c.2253G>T
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NP_001369734.1:p.Glu751Asp
|
|
NM_001382806.1:c.2166G>T
|
NP_001369735.1:p.Glu722Asp
|
|
NM_004448.4:c.3204G>T
MANE Select
|
NP_004439.2:p.Glu1068Asp
|
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NR_110535.2:n.3442G>T
|
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