|
ENST00000703936.1:c.2737T>G
|
ENSP00000515567.1:p.Tyr913Asp
|
|
|
ENST00000703937.1:c.*1798T>G
|
ENSP00000515568.1:n.*1798T>G
|
|
|
ENST00000326739.9:c.697T>G
MANE Select
|
ENSP00000321584.4:p.Tyr233Asp
|
|
|
ENST00000429182.6:c.697T>G
|
ENSP00000393525.2:p.Tyr233Asp
|
|
|
ENST00000442157.2:c.622T>G
|
ENSP00000403502.2:p.Tyr208Asp
|
|
|
ENST00000462980.2:n.1212T>G
|
|
|
|
ENST00000472328.2:n.763T>G
|
|
|
|
ENST00000491610.2:n.657T>G
|
|
|
|
ENST00000676607.1:n.993T>G
|
|
|
|
ENST00000676627.1:n.1427T>G
|
|
|
|
ENST00000676708.1:n.1977T>G
|
|
|
|
ENST00000676864.1:n.1846T>G
|
|
|
|
ENST00000677010.1:c.733T>G
|
ENSP00000503089.1:p.Tyr245Asp
|
|
|
ENST00000677108.1:n.2603T>G
|
|
|
|
ENST00000677168.1:n.1169T>G
|
|
|
|
ENST00000677185.1:n.1260T>G
|
|
|
|
ENST00000677205.1:n.1481T>G
|
|
|
|
ENST00000677344.1:n.1971T>G
|
|
|
|
ENST00000677480.1:c.*374T>G
|
ENSP00000504378.1:n.*374T>G
|
|
|
ENST00000677519.1:n.1407T>G
|
|
|
|
ENST00000677593.1:n.1253T>G
|
|
|
|
ENST00000677740.1:n.2202T>G
|
|
|
|
ENST00000677991.1:n.1870T>G
|
|
|
|
ENST00000678001.1:n.1190T>G
|
|
|
|
ENST00000678085.1:n.1253T>G
|
|
|
|
ENST00000678177.1:n.2546T>G
|
|
|
|
ENST00000678603.1:n.1775T>G
|
|
|
|
ENST00000678724.1:c.622T>G
|
ENSP00000503874.1:p.Tyr208Asp
|
|
|
ENST00000678920.1:n.855T>G
|
|
|
|
ENST00000679019.1:n.1467T>G
|
|
|
|
ENST00000679117.1:c.*512T>G
|
ENSP00000503240.1:n.*512T>G
|
|
|
ENST00000679339.1:n.1538T>G
|
|
|
|
ENST00000326739.8:c.697T>G
|
ENSP00000321584.4:p.Tyr233Asp
|
|
|
ENST00000429182.5:c.491T>G
|
|
|
|
ENST00000442157.1:c.622T>G
|
ENSP00000403502.1:p.Tyr208Asp
|
|
|
ENST00000462980.1:n.599T>G
|
|
|
|
ENST00000491610.1:n.657T>G
|
|
|
|
NM_000884.2:c.697T>G
|
NP_000875.2:p.Tyr233Asp
|
|
|
XM_006713128.2:c.907T>G
|
XP_006713191.1:p.Tyr303Asp
|
|
|
XM_006713128.3:c.907T>G
|
XP_006713191.1:p.Tyr303Asp
|
|
|
XM_017006349.1:c.832T>G
|
XP_016861838.1:p.Tyr278Asp
|
|
|
XM_017006350.1:c.832T>G
|
XP_016861839.1:p.Tyr278Asp
|
|
|
NM_000884.3:c.697T>G
MANE Select
|
NP_000875.2:p.Tyr233Asp
|
|
