ENST00000269571.10:c.3653A>T
MANE Select
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ENSP00000269571.4:p.Asp1218Val
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ENST00000269571.9:c.3653A>T
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ENSP00000269571.4:p.Asp1218Val
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ENST00000406381.6:c.3563A>T
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ENSP00000385185.2:p.Asp1188Val
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ENST00000445658.6:c.2825A>T
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ENSP00000404047.2:p.Asp942Val
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ENST00000541774.5:c.3608A>T
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ENSP00000446466.1:p.Asp1203Val
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ENST00000578373.5:c.*3443A>T
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ENSP00000463427.1:n.*3443A>T
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ENST00000584450.5:c.*232A>T
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ENSP00000463714.1:n.*232A>T
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ENST00000584601.5:c.3563A>T
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ENSP00000462438.1:p.Asp1188Val
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NM_001005862.2:c.3563A>T , LRG_724t1:c.3563A>T
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NP_001005862.1:p.Asp1188Val
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NM_001289936.1:c.3608A>T , LRG_724t4:c.3608A>T
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NP_001276865.1:p.Asp1203Val
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NM_001289937.1:c.*232A>T
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NP_001276866.1:n.*232A>T
|
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NM_004448.3:c.3653A>T , LRG_724t2:c.3653A>T
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NP_004439.2:p.Asp1218Val
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|
NR_110535.1:n.3977A>T
|
|
|
XM_024450641.1:c.3791A>T
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XP_024306409.1:p.Asp1264Val
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XM_024450642.1:c.3746A>T
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XP_024306410.1:p.Asp1249Val
|
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XM_024450643.1:c.3701A>T
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XP_024306411.1:p.Asp1234Val
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NM_001005862.3:c.3563A>T
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NP_001005862.1:p.Asp1188Val
|
|
NM_001289936.2:c.3608A>T
|
NP_001276865.1:p.Asp1203Val
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NM_001289937.2:c.*232A>T
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NP_001276866.1:n.*232A>T
|
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NM_001382782.1:c.3563A>T
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NP_001369711.1:p.Asp1188Val
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NM_001382783.1:c.3563A>T
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NP_001369712.1:p.Asp1188Val
|
|
NM_001382784.1:c.3770A>T
|
NP_001369713.1:p.Asp1257Val
|
|
NM_001382785.1:c.3755A>T
|
NP_001369714.1:p.Asp1252Val
|
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NM_001382786.1:c.3734A>T
|
NP_001369715.1:p.Asp1245Val
|
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NM_001382787.1:c.3728A>T
|
NP_001369716.1:p.Asp1243Val
|
|
NM_001382788.1:c.3683A>T
|
NP_001369717.1:p.Asp1228Val
|
|
NM_001382789.1:c.3674A>T
|
NP_001369718.1:p.Asp1225Val
|
|
NM_001382790.1:c.3650A>T
|
NP_001369719.1:p.Asp1217Val
|
|
NM_001382791.1:c.3644A>T
|
NP_001369720.1:p.Asp1215Val
|
|
NM_001382792.1:c.3617A>T
|
NP_001369721.1:p.Asp1206Val
|
|
NM_001382793.1:c.3611A>T
|
NP_001369722.1:p.Asp1204Val
|
|
NM_001382794.1:c.3611A>T
|
NP_001369723.1:p.Asp1204Val
|
|
NM_001382795.1:c.3605A>T
|
NP_001369724.1:p.Asp1202Val
|
|
NM_001382796.1:c.3566A>T
|
NP_001369725.1:p.Asp1189Val
|
|
NM_001382797.1:c.3554A>T
|
NP_001369726.1:p.Asp1185Val
|
|
NM_001382798.1:c.3497A>T
|
NP_001369727.1:p.Asp1166Val
|
|
NM_001382799.1:c.3473A>T
|
NP_001369728.1:p.Asp1158Val
|
|
NM_001382800.1:c.3467A>T
|
NP_001369729.1:p.Asp1156Val
|
|
NM_001382801.1:c.3449A>T
|
NP_001369730.1:p.Asp1150Val
|
|
NM_001382802.1:c.3395A>T
|
NP_001369731.1:p.Asp1132Val
|
|
NM_001382803.1:c.*232A>T
|
NP_001369732.1:n.*232A>T
|
|
NM_001382804.1:c.2825A>T
|
NP_001369733.1:p.Asp942Val
|
|
NM_001382805.1:c.2702A>T
|
NP_001369734.1:p.Asp901Val
|
|
NM_001382806.1:c.2615A>T
|
NP_001369735.1:p.Asp872Val
|
|
NM_004448.4:c.3653A>T
MANE Select
|
NP_004439.2:p.Asp1218Val
|
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NR_110535.2:n.3891A>T
|
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