ENST00000269571.10:c.3504A>T
MANE Select
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ENSP00000269571.4:p.Glu1168Asp
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ENST00000269571.9:c.3504A>T
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ENSP00000269571.4:p.Glu1168Asp
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ENST00000406381.6:c.3414A>T
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ENSP00000385185.2:p.Glu1138Asp
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ENST00000445658.6:c.2676A>T
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ENSP00000404047.2:p.Glu892Asp
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ENST00000541774.5:c.3459A>T
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ENSP00000446466.1:p.Glu1153Asp
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ENST00000578373.5:c.*3294A>T
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ENSP00000463427.1:n.*3294A>T
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ENST00000584450.5:c.*83A>T
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ENSP00000463714.1:n.*83A>T
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ENST00000584601.5:c.3414A>T
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ENSP00000462438.1:p.Glu1138Asp
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NM_001005862.2:c.3414A>T , LRG_724t1:c.3414A>T
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NP_001005862.1:p.Glu1138Asp
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NM_001289936.1:c.3459A>T , LRG_724t4:c.3459A>T
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NP_001276865.1:p.Glu1153Asp
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NM_001289937.1:c.*83A>T
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NP_001276866.1:n.*83A>T
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NM_004448.3:c.3504A>T , LRG_724t2:c.3504A>T
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NP_004439.2:p.Glu1168Asp
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NR_110535.1:n.3828A>T
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XM_024450641.1:c.3642A>T
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XP_024306409.1:p.Glu1214Asp
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XM_024450642.1:c.3597A>T
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XP_024306410.1:p.Glu1199Asp
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XM_024450643.1:c.3552A>T
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XP_024306411.1:p.Glu1184Asp
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NM_001005862.3:c.3414A>T
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NP_001005862.1:p.Glu1138Asp
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NM_001289936.2:c.3459A>T
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NP_001276865.1:p.Glu1153Asp
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NM_001289937.2:c.*83A>T
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NP_001276866.1:n.*83A>T
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NM_001382782.1:c.3414A>T
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NP_001369711.1:p.Glu1138Asp
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NM_001382783.1:c.3414A>T
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NP_001369712.1:p.Glu1138Asp
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NM_001382784.1:c.3621A>T
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NP_001369713.1:p.Glu1207Asp
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NM_001382785.1:c.3606A>T
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NP_001369714.1:p.Glu1202Asp
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NM_001382786.1:c.3585A>T
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NP_001369715.1:p.Glu1195Asp
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NM_001382787.1:c.3579A>T
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NP_001369716.1:p.Glu1193Asp
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NM_001382788.1:c.3534A>T
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NP_001369717.1:p.Glu1178Asp
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NM_001382789.1:c.3525A>T
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NP_001369718.1:p.Glu1175Asp
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NM_001382790.1:c.3501A>T
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NP_001369719.1:p.Glu1167Asp
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NM_001382791.1:c.3495A>T
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NP_001369720.1:p.Glu1165Asp
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NM_001382792.1:c.3468A>T
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NP_001369721.1:p.Glu1156Asp
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NM_001382793.1:c.3462A>T
|
NP_001369722.1:p.Glu1154Asp
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NM_001382794.1:c.3462A>T
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NP_001369723.1:p.Glu1154Asp
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NM_001382795.1:c.3456A>T
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NP_001369724.1:p.Glu1152Asp
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NM_001382796.1:c.3417A>T
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NP_001369725.1:p.Glu1139Asp
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NM_001382797.1:c.3405A>T
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NP_001369726.1:p.Glu1135Asp
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NM_001382798.1:c.3348A>T
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NP_001369727.1:p.Glu1116Asp
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NM_001382799.1:c.3324A>T
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NP_001369728.1:p.Glu1108Asp
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NM_001382800.1:c.3318A>T
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NP_001369729.1:p.Glu1106Asp
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NM_001382801.1:c.3300A>T
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NP_001369730.1:p.Glu1100Asp
|
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NM_001382802.1:c.3246A>T
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NP_001369731.1:p.Glu1082Asp
|
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NM_001382803.1:c.*83A>T
|
NP_001369732.1:n.*83A>T
|
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NM_001382804.1:c.2676A>T
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NP_001369733.1:p.Glu892Asp
|
|
NM_001382805.1:c.2553A>T
|
NP_001369734.1:p.Glu851Asp
|
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NM_001382806.1:c.2466A>T
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NP_001369735.1:p.Glu822Asp
|
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NM_004448.4:c.3504A>T
MANE Select
|
NP_004439.2:p.Glu1168Asp
|
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NR_110535.2:n.3742A>T
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