ENST00000269571.10:c.3548A>T
MANE Select
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ENSP00000269571.4:p.Asp1183Val
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ENST00000269571.9:c.3548A>T
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ENSP00000269571.4:p.Asp1183Val
|
|
ENST00000406381.6:c.3458A>T
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ENSP00000385185.2:p.Asp1153Val
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ENST00000445658.6:c.2720A>T
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ENSP00000404047.2:p.Asp907Val
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ENST00000541774.5:c.3503A>T
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ENSP00000446466.1:p.Asp1168Val
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ENST00000578373.5:c.*3338A>T
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ENSP00000463427.1:n.*3338A>T
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ENST00000584450.5:c.*127A>T
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ENSP00000463714.1:n.*127A>T
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ENST00000584601.5:c.3458A>T
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ENSP00000462438.1:p.Asp1153Val
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NM_001005862.2:c.3458A>T , LRG_724t1:c.3458A>T
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NP_001005862.1:p.Asp1153Val
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NM_001289936.1:c.3503A>T , LRG_724t4:c.3503A>T
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NP_001276865.1:p.Asp1168Val
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NM_001289937.1:c.*127A>T
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NP_001276866.1:n.*127A>T
|
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NM_004448.3:c.3548A>T , LRG_724t2:c.3548A>T
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NP_004439.2:p.Asp1183Val
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NR_110535.1:n.3872A>T
|
|
|
XM_024450641.1:c.3686A>T
|
XP_024306409.1:p.Asp1229Val
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XM_024450642.1:c.3641A>T
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XP_024306410.1:p.Asp1214Val
|
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XM_024450643.1:c.3596A>T
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XP_024306411.1:p.Asp1199Val
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NM_001005862.3:c.3458A>T
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NP_001005862.1:p.Asp1153Val
|
|
NM_001289936.2:c.3503A>T
|
NP_001276865.1:p.Asp1168Val
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NM_001289937.2:c.*127A>T
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NP_001276866.1:n.*127A>T
|
|
NM_001382782.1:c.3458A>T
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NP_001369711.1:p.Asp1153Val
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NM_001382783.1:c.3458A>T
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NP_001369712.1:p.Asp1153Val
|
|
NM_001382784.1:c.3665A>T
|
NP_001369713.1:p.Asp1222Val
|
|
NM_001382785.1:c.3650A>T
|
NP_001369714.1:p.Asp1217Val
|
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NM_001382786.1:c.3629A>T
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NP_001369715.1:p.Asp1210Val
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NM_001382787.1:c.3623A>T
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NP_001369716.1:p.Asp1208Val
|
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NM_001382788.1:c.3578A>T
|
NP_001369717.1:p.Asp1193Val
|
|
NM_001382789.1:c.3569A>T
|
NP_001369718.1:p.Asp1190Val
|
|
NM_001382790.1:c.3545A>T
|
NP_001369719.1:p.Asp1182Val
|
|
NM_001382791.1:c.3539A>T
|
NP_001369720.1:p.Asp1180Val
|
|
NM_001382792.1:c.3512A>T
|
NP_001369721.1:p.Asp1171Val
|
|
NM_001382793.1:c.3506A>T
|
NP_001369722.1:p.Asp1169Val
|
|
NM_001382794.1:c.3506A>T
|
NP_001369723.1:p.Asp1169Val
|
|
NM_001382795.1:c.3500A>T
|
NP_001369724.1:p.Asp1167Val
|
|
NM_001382796.1:c.3461A>T
|
NP_001369725.1:p.Asp1154Val
|
|
NM_001382797.1:c.3449A>T
|
NP_001369726.1:p.Asp1150Val
|
|
NM_001382798.1:c.3392A>T
|
NP_001369727.1:p.Asp1131Val
|
|
NM_001382799.1:c.3368A>T
|
NP_001369728.1:p.Asp1123Val
|
|
NM_001382800.1:c.3362A>T
|
NP_001369729.1:p.Asp1121Val
|
|
NM_001382801.1:c.3344A>T
|
NP_001369730.1:p.Asp1115Val
|
|
NM_001382802.1:c.3290A>T
|
NP_001369731.1:p.Asp1097Val
|
|
NM_001382803.1:c.*127A>T
|
NP_001369732.1:n.*127A>T
|
|
NM_001382804.1:c.2720A>T
|
NP_001369733.1:p.Asp907Val
|
|
NM_001382805.1:c.2597A>T
|
NP_001369734.1:p.Asp866Val
|
|
NM_001382806.1:c.2510A>T
|
NP_001369735.1:p.Asp837Val
|
|
NM_004448.4:c.3548A>T
MANE Select
|
NP_004439.2:p.Asp1183Val
|
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NR_110535.2:n.3786A>T
|
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