ENST00000374647.10:c.2737G>T
MANE Select
|
ENSP00000363779.5:p.Asp913Tyr
|
|
ENST00000495759.6:c.*1347G>T
|
ENSP00000433514.2:n.*1347G>T
|
|
ENST00000674535.1:c.2737G>T
|
ENSP00000502142.1:p.Asp913Tyr
|
|
ENST00000674704.1:n.5822G>T
|
|
|
ENST00000674836.1:n.3350G>T
|
|
|
ENST00000674890.1:c.2759G>T
|
ENSP00000501870.1:p.Gly920Val
|
|
ENST00000674938.1:c.2395G>T
|
ENSP00000502427.1:p.Asp799Tyr
|
|
ENST00000674948.1:c.2395G>T
|
ENSP00000501602.1:p.Asp799Tyr
|
|
ENST00000675052.1:c.2737G>T
|
ENSP00000502664.1:p.Asp913Tyr
|
|
ENST00000675078.1:c.2737G>T
|
ENSP00000501549.1:p.Asp913Tyr
|
|
ENST00000675215.1:c.*1961G>T
|
ENSP00000502558.1:n.*1961G>T
|
|
ENST00000675233.1:n.4564G>T
|
|
|
ENST00000675321.1:c.2737G>T
|
ENSP00000502751.1:p.Asp913Tyr
|
|
ENST00000675325.1:n.4694G>T
|
|
|
ENST00000675335.1:c.2768G>T
|
ENSP00000502182.1:n.2768G>T
|
|
ENST00000675400.1:n.4472G>T
|
|
|
ENST00000675406.1:c.2737G>T
|
ENSP00000501893.1:p.Asp913Tyr
|
|
ENST00000675458.1:c.2830G>T
|
ENSP00000501754.1:n.2830G>T
|
|
ENST00000675507.1:n.4533G>T
|
|
|
ENST00000675535.1:c.*364G>T
|
ENSP00000501667.1:n.*364G>T
|
|
ENST00000675566.1:n.4595G>T
|
|
|
ENST00000675602.1:n.5785G>T
|
|
|
ENST00000675647.1:n.3042G>T
|
|
|
ENST00000675711.1:c.2737G>T
|
ENSP00000502485.1:p.Asp913Tyr
|
|
ENST00000675727.1:c.2737G>T
|
ENSP00000501722.1:p.Asp913Tyr
|
|
ENST00000675748.1:n.4371G>T
|
|
|
ENST00000675765.1:c.*120G>T
|
ENSP00000502640.1:n.*120G>T
|
|
ENST00000675825.1:c.2737G>T
|
ENSP00000502632.1:p.Asp913Tyr
|
|
ENST00000675877.1:n.3042G>T
|
|
|
ENST00000675893.1:c.*3806G>T
|
ENSP00000502001.1:n.*3806G>T
|
|
ENST00000675943.1:n.6352G>T
|
|
|
ENST00000675979.1:c.*1980G>T
|
ENSP00000502208.1:n.*1980G>T
|
|
ENST00000676044.1:c.*397G>T
|
ENSP00000502378.1:n.*397G>T
|
|
ENST00000676086.1:n.4522G>T
|
|
|
ENST00000676121.1:n.4565G>T
|
|
|
ENST00000676237.1:c.2638G>T
|
ENSP00000501828.1:p.Asp880Tyr
|
|
ENST00000676416.1:c.2395G>T
|
ENSP00000501660.1:p.Asp799Tyr
|
|
ENST00000676424.1:n.4533G>T
|
|
|
ENST00000676429.1:n.7206G>T
|
|
|
ENST00000374647.9:c.2737G>T
|
ENSP00000363779.5:p.Asp913Tyr
|
|
ENST00000537196.1:c.1690G>T
|
ENSP00000439367.1:p.Asp564Tyr
|
|
NM_003640.3:c.2737G>T , LRG_251t1:c.2737G>T
|
NP_003631.2:p.Asp913Tyr
|
|
XM_005252285.2:c.2395G>T
|
XP_005252342.1:p.Asp799Tyr
|
|
XM_011519136.1:c.2737G>T
|
XP_011517438.1:p.Asp913Tyr
|
|
XM_011519137.1:c.2395G>T
|
XP_011517439.1:p.Asp799Tyr
|
|
XR_929859.1:n.3115G>T
|
|
|
NM_001318360.1:c.2395G>T
|
NP_001305289.1:p.Asp799Tyr
|
|
NM_001330749.1:c.1690G>T
|
NP_001317678.1:p.Asp564Tyr
|
|
NM_003640.4:c.2737G>T
|
NP_003631.2:p.Asp913Tyr
|
|
XM_011519136.2:c.2737G>T
|
XP_011517438.1:p.Asp913Tyr
|
|
XR_929859.3:n.3126G>T
|
|
|
NM_003640.5:c.2737G>T
MANE Select
|
NP_003631.2:p.Asp913Tyr
|
|
NM_001318360.2:c.2395G>T
|
NP_001305289.1:p.Asp799Tyr
|
|
NM_001330749.2:c.1690G>T
|
NP_001317678.1:p.Asp564Tyr
|
|