ENST00000374647.10:c.3463G>T
MANE Select
|
ENSP00000363779.5:p.Asp1155Tyr
|
|
ENST00000495759.6:c.*2073G>T
|
ENSP00000433514.2:n.*2073G>T
|
|
ENST00000674535.1:c.3463G>T
|
ENSP00000502142.1:p.Asp1155Tyr
|
|
ENST00000674704.1:n.6548G>T
|
|
|
ENST00000674740.1:n.346G>T
|
|
|
ENST00000674836.1:n.4076G>T
|
|
|
ENST00000674890.1:c.*698G>T
|
ENSP00000501870.1:n.*698G>T
|
|
ENST00000674938.1:c.3121G>T
|
ENSP00000502427.1:p.Asp1041Tyr
|
|
ENST00000674948.1:c.3121G>T
|
ENSP00000501602.1:p.Asp1041Tyr
|
|
ENST00000675052.1:c.3463G>T
|
ENSP00000502664.1:p.Asp1155Tyr
|
|
ENST00000675062.1:n.509G>T
|
|
|
ENST00000675078.1:c.3463G>T
|
ENSP00000501549.1:p.Asp1155Tyr
|
|
ENST00000675215.1:c.*2687G>T
|
ENSP00000502558.1:n.*2687G>T
|
|
ENST00000675233.1:n.5290G>T
|
|
|
ENST00000675321.1:c.3460+497G>T
|
ENSP00000502751.1:n.3460+497G>T
|
|
ENST00000675325.1:n.5420G>T
|
|
|
ENST00000675335.1:c.3494G>T
|
ENSP00000502182.1:n.3494G>T
|
|
ENST00000675400.1:n.5315G>T
|
|
|
ENST00000675406.1:c.3463G>T
|
ENSP00000501893.1:p.Asp1155Tyr
|
|
ENST00000675458.1:c.3556G>T
|
ENSP00000501754.1:n.3556G>T
|
|
ENST00000675507.1:n.5259G>T
|
|
|
ENST00000675535.1:c.*1090G>T
|
ENSP00000501667.1:n.*1090G>T
|
|
ENST00000675566.1:n.5321G>T
|
|
|
ENST00000675580.1:n.616G>T
|
|
|
ENST00000675602.1:n.6511G>T
|
|
|
ENST00000675647.1:n.4627G>T
|
|
|
ENST00000675711.1:c.3580G>T
|
ENSP00000502485.1:n.3580G>T
|
|
ENST00000675727.1:c.3463G>T
|
ENSP00000501722.1:p.Asp1155Tyr
|
|
ENST00000675748.1:n.5097G>T
|
|
|
ENST00000675765.1:c.*846G>T
|
ENSP00000502640.1:n.*846G>T
|
|
ENST00000675825.1:c.3505G>T
|
ENSP00000502632.1:p.Asp1169Tyr
|
|
ENST00000675877.1:n.5307G>T
|
|
|
ENST00000675893.1:c.*4532G>T
|
ENSP00000502001.1:n.*4532G>T
|
|
ENST00000675943.1:n.7078G>T
|
|
|
ENST00000675979.1:c.*2706G>T
|
ENSP00000502208.1:n.*2706G>T
|
|
ENST00000676044.1:c.*1123G>T
|
ENSP00000502378.1:n.*1123G>T
|
|
ENST00000676086.1:n.5248G>T
|
|
|
ENST00000676121.1:n.5291G>T
|
|
|
ENST00000676162.1:n.192G>T
|
|
|
ENST00000676237.1:c.3406G>T
|
ENSP00000501828.1:p.Asp1136Tyr
|
|
ENST00000676416.1:c.3163G>T
|
ENSP00000501660.1:p.Asp1055Tyr
|
|
ENST00000676424.1:n.5301G>T
|
|
|
ENST00000676429.1:n.7932G>T
|
|
|
ENST00000374647.9:c.3463G>T
|
ENSP00000363779.5:p.Asp1155Tyr
|
|
ENST00000467959.1:n.343G>T
|
|
|
ENST00000495759.5:c.603G>T
|
|
|
ENST00000537196.1:c.2416G>T
|
ENSP00000439367.1:p.Asp806Tyr
|
|
NM_003640.3:c.3463G>T , LRG_251t1:c.3463G>T
|
NP_003631.2:p.Asp1155Tyr
|
|
XM_005252285.2:c.3121G>T
|
XP_005252342.1:p.Asp1041Tyr
|
|
XM_011519136.1:c.3505G>T
|
XP_011517438.1:p.Asp1169Tyr
|
|
XM_011519137.1:c.3163G>T
|
XP_011517439.1:p.Asp1055Tyr
|
|
NM_001318360.1:c.3121G>T
|
NP_001305289.1:p.Asp1041Tyr
|
|
NM_001330749.1:c.2416G>T
|
NP_001317678.1:p.Asp806Tyr
|
|
NM_003640.4:c.3463G>T
|
NP_003631.2:p.Asp1155Tyr
|
|
XM_011519136.2:c.3505G>T
|
XP_011517438.1:p.Asp1169Tyr
|
|
XR_929859.3:n.3852G>T
|
|
|
NM_003640.5:c.3463G>T
MANE Select
|
NP_003631.2:p.Asp1155Tyr
|
|
NM_001318360.2:c.3121G>T
|
NP_001305289.1:p.Asp1041Tyr
|
|
NM_001330749.2:c.2416G>T
|
NP_001317678.1:p.Asp806Tyr
|
|