|
ENST00000700029.2:c.1210_1212delinsTAT
|
ENSP00000514759.2:p.Glu404Tyr
|
|
|
ENST00000710265.1:c.*146_*148delinsTAT
|
ENSP00000518161.1:n.*146_*148delinsTAT
|
|
|
ENST00000688158.2:n.1852_1854delinsTAT
|
|
|
|
ENST00000688922.2:c.*947_*949delinsTAT
|
ENSP00000508742.2:n.*947_*949delinsTAT
|
|
|
ENST00000700021.1:c.1072_1074delinsTAT
|
ENSP00000514757.1:p.Glu358Tyr
|
|
|
ENST00000700022.1:c.*456_*458delinsTAT
|
ENSP00000514758.1:n.*456_*458delinsTAT
|
|
|
ENST00000700023.1:n.2275_2277delinsTAT
|
|
|
|
ENST00000700024.1:n.2509_2511delinsTAT
|
|
|
|
ENST00000706954.1:c.1117_1119delinsTAT
|
ENSP00000516674.1:p.Glu373Tyr
|
|
|
ENST00000706955.1:c.*1152_*1154delinsTAT
|
ENSP00000516675.1:n.*1152_*1154delinsTAT
|
|
|
ENST00000686459.1:c.*703_*705delinsTAT
|
ENSP00000508909.1:n.*703_*705delinsTAT
|
|
|
ENST00000688158.1:c.*1228_*1230delinsTAT
|
ENSP00000509254.1:n.*1228_*1230delinsTAT
|
|
|
ENST00000688308.1:c.1117_1119delinsTAT
|
ENSP00000508752.1:p.Glu373Tyr
|
|
|
ENST00000688922.1:c.1038_1040delinsTAT
|
|
|
|
ENST00000693560.1:c.1636_1638delinsTAT
|
ENSP00000509861.1:p.Glu546Tyr
|
|
|
ENST00000371953.8:c.1117_1119delinsTAT
MANE Select
|
ENSP00000361021.3:p.Glu373Tyr
|
|
|
ENST00000371953.7:c.1117_1119delinsTAT
|
ENSP00000361021.3:p.Glu373Tyr
|
|
|
NM_000314.5:c.1117_1119delinsTAT
|
NP_000305.3:p.Glu373Tyr
|
|
|
NM_000314.6:c.1117_1119delinsTAT
|
NP_000305.3:p.Glu373Tyr
|
|
|
NM_001304717.2:c.1636_1638delinsTAT
|
NP_001291646.2:p.Glu546Tyr
|
|
|
NM_001304718.1:c.526_528delinsTAT
|
NP_001291647.1:p.Glu176Tyr
|
|
|
XM_006717926.2:c.1072_1074delinsTAT
|
XP_006717989.1:p.Glu358Tyr
|
|
|
XM_011539982.1:c.1021_1023delinsTAT
|
XP_011538284.1:p.Glu341Tyr
|
|
|
XR_945791.1:n.1687_1689delinsTAT
|
|
|
|
NM_000314.7:c.1117_1119delinsTAT
|
NP_000305.3:p.Glu373Tyr
|
|
|
NM_001304717.5:c.1636_1638delinsTAT
|
NP_001291646.4:p.Glu546Tyr
|
|
|
NM_001304718.2:c.526_528delinsTAT
|
NP_001291647.1:p.Glu176Tyr
|
|
|
NM_000314.8:c.1117_1119delinsTAT
MANE Select
|
NP_000305.3:p.Glu373Tyr
|
|
