ENST00000269571.10:c.3551T>A
MANE Select
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ENSP00000269571.4:p.Val1184Asp
|
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ENST00000269571.9:c.3551T>A
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ENSP00000269571.4:p.Val1184Asp
|
|
ENST00000406381.6:c.3461T>A
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ENSP00000385185.2:p.Val1154Asp
|
|
ENST00000445658.6:c.2723T>A
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ENSP00000404047.2:p.Val908Asp
|
|
ENST00000541774.5:c.3506T>A
|
ENSP00000446466.1:p.Val1169Asp
|
|
ENST00000578373.5:c.*3341T>A
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ENSP00000463427.1:n.*3341T>A
|
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ENST00000584450.5:c.*130T>A
|
ENSP00000463714.1:n.*130T>A
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|
ENST00000584601.5:c.3461T>A
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ENSP00000462438.1:p.Val1154Asp
|
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NM_001005862.2:c.3461T>A , LRG_724t1:c.3461T>A
|
NP_001005862.1:p.Val1154Asp
|
|
NM_001289936.1:c.3506T>A , LRG_724t4:c.3506T>A
|
NP_001276865.1:p.Val1169Asp
|
|
NM_001289937.1:c.*130T>A
|
NP_001276866.1:n.*130T>A
|
|
NM_004448.3:c.3551T>A , LRG_724t2:c.3551T>A
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NP_004439.2:p.Val1184Asp
|
|
NR_110535.1:n.3875T>A
|
|
|
XM_024450641.1:c.3689T>A
|
XP_024306409.1:p.Val1230Asp
|
|
XM_024450642.1:c.3644T>A
|
XP_024306410.1:p.Val1215Asp
|
|
XM_024450643.1:c.3599T>A
|
XP_024306411.1:p.Val1200Asp
|
|
NM_001005862.3:c.3461T>A
|
NP_001005862.1:p.Val1154Asp
|
|
NM_001289936.2:c.3506T>A
|
NP_001276865.1:p.Val1169Asp
|
|
NM_001289937.2:c.*130T>A
|
NP_001276866.1:n.*130T>A
|
|
NM_001382782.1:c.3461T>A
|
NP_001369711.1:p.Val1154Asp
|
|
NM_001382783.1:c.3461T>A
|
NP_001369712.1:p.Val1154Asp
|
|
NM_001382784.1:c.3668T>A
|
NP_001369713.1:p.Val1223Asp
|
|
NM_001382785.1:c.3653T>A
|
NP_001369714.1:p.Val1218Asp
|
|
NM_001382786.1:c.3632T>A
|
NP_001369715.1:p.Val1211Asp
|
|
NM_001382787.1:c.3626T>A
|
NP_001369716.1:p.Val1209Asp
|
|
NM_001382788.1:c.3581T>A
|
NP_001369717.1:p.Val1194Asp
|
|
NM_001382789.1:c.3572T>A
|
NP_001369718.1:p.Val1191Asp
|
|
NM_001382790.1:c.3548T>A
|
NP_001369719.1:p.Val1183Asp
|
|
NM_001382791.1:c.3542T>A
|
NP_001369720.1:p.Val1181Asp
|
|
NM_001382792.1:c.3515T>A
|
NP_001369721.1:p.Val1172Asp
|
|
NM_001382793.1:c.3509T>A
|
NP_001369722.1:p.Val1170Asp
|
|
NM_001382794.1:c.3509T>A
|
NP_001369723.1:p.Val1170Asp
|
|
NM_001382795.1:c.3503T>A
|
NP_001369724.1:p.Val1168Asp
|
|
NM_001382796.1:c.3464T>A
|
NP_001369725.1:p.Val1155Asp
|
|
NM_001382797.1:c.3452T>A
|
NP_001369726.1:p.Val1151Asp
|
|
NM_001382798.1:c.3395T>A
|
NP_001369727.1:p.Val1132Asp
|
|
NM_001382799.1:c.3371T>A
|
NP_001369728.1:p.Val1124Asp
|
|
NM_001382800.1:c.3365T>A
|
NP_001369729.1:p.Val1122Asp
|
|
NM_001382801.1:c.3347T>A
|
NP_001369730.1:p.Val1116Asp
|
|
NM_001382802.1:c.3293T>A
|
NP_001369731.1:p.Val1098Asp
|
|
NM_001382803.1:c.*130T>A
|
NP_001369732.1:n.*130T>A
|
|
NM_001382804.1:c.2723T>A
|
NP_001369733.1:p.Val908Asp
|
|
NM_001382805.1:c.2600T>A
|
NP_001369734.1:p.Val867Asp
|
|
NM_001382806.1:c.2513T>A
|
NP_001369735.1:p.Val838Asp
|
|
NM_004448.4:c.3551T>A
MANE Select
|
NP_004439.2:p.Val1184Asp
|
|
NR_110535.2:n.3789T>A
|
|
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