|
ENST00000703936.1:c.2813A>C
|
ENSP00000515567.1:p.Tyr938Ser
|
|
|
ENST00000703937.1:c.*1874A>C
|
ENSP00000515568.1:n.*1874A>C
|
|
|
ENST00000326739.9:c.773A>C
MANE Select
|
ENSP00000321584.4:p.Tyr258Ser
|
|
|
ENST00000429182.6:c.773A>C
|
ENSP00000393525.2:p.Tyr258Ser
|
|
|
ENST00000442157.2:c.698A>C
|
ENSP00000403502.2:p.Tyr233Ser
|
|
|
ENST00000462980.2:n.1288A>C
|
|
|
|
ENST00000472328.2:n.839A>C
|
|
|
|
ENST00000491610.2:n.733A>C
|
|
|
|
ENST00000676607.1:n.1069A>C
|
|
|
|
ENST00000676627.1:n.1503A>C
|
|
|
|
ENST00000676708.1:n.2053A>C
|
|
|
|
ENST00000676864.1:n.1922A>C
|
|
|
|
ENST00000677010.1:c.809A>C
|
ENSP00000503089.1:p.Tyr270Ser
|
|
|
ENST00000677108.1:n.2679A>C
|
|
|
|
ENST00000677168.1:n.1245A>C
|
|
|
|
ENST00000677185.1:n.1336A>C
|
|
|
|
ENST00000677205.1:n.1557A>C
|
|
|
|
ENST00000677344.1:n.2047A>C
|
|
|
|
ENST00000677480.1:c.*450A>C
|
ENSP00000504378.1:n.*450A>C
|
|
|
ENST00000677519.1:n.1483A>C
|
|
|
|
ENST00000677593.1:n.1329A>C
|
|
|
|
ENST00000677740.1:n.2278A>C
|
|
|
|
ENST00000677991.1:n.1946A>C
|
|
|
|
ENST00000678001.1:n.1266A>C
|
|
|
|
ENST00000678085.1:n.1329A>C
|
|
|
|
ENST00000678177.1:n.2622A>C
|
|
|
|
ENST00000678603.1:n.1851A>C
|
|
|
|
ENST00000678724.1:c.698A>C
|
ENSP00000503874.1:p.Tyr233Ser
|
|
|
ENST00000678920.1:n.931A>C
|
|
|
|
ENST00000679019.1:n.1543A>C
|
|
|
|
ENST00000679117.1:c.*588A>C
|
ENSP00000503240.1:n.*588A>C
|
|
|
ENST00000679339.1:n.1614A>C
|
|
|
|
ENST00000326739.8:c.773A>C
|
ENSP00000321584.4:p.Tyr258Ser
|
|
|
ENST00000429182.5:c.567A>C
|
|
|
|
ENST00000442157.1:c.698A>C
|
ENSP00000403502.1:p.Tyr233Ser
|
|
|
ENST00000462980.1:n.675A>C
|
|
|
|
ENST00000491610.1:n.733A>C
|
|
|
|
NM_000884.2:c.773A>C
|
NP_000875.2:p.Tyr258Ser
|
|
|
XM_006713128.2:c.983A>C
|
XP_006713191.1:p.Tyr328Ser
|
|
|
XM_006713128.3:c.983A>C
|
XP_006713191.1:p.Tyr328Ser
|
|
|
XM_017006349.1:c.908A>C
|
XP_016861838.1:p.Tyr303Ser
|
|
|
XM_017006350.1:c.908A>C
|
XP_016861839.1:p.Tyr303Ser
|
|
|
NM_000884.3:c.773A>C
MANE Select
|
NP_000875.2:p.Tyr258Ser
|
|
