|
ENST00000703936.1:c.2795C>G
|
ENSP00000515567.1:p.Thr932Ser
|
|
|
ENST00000703937.1:c.*1856C>G
|
ENSP00000515568.1:n.*1856C>G
|
|
|
ENST00000326739.9:c.755C>G
MANE Select
|
ENSP00000321584.4:p.Thr252Ser
|
|
|
ENST00000429182.6:c.755C>G
|
ENSP00000393525.2:p.Thr252Ser
|
|
|
ENST00000442157.2:c.680C>G
|
ENSP00000403502.2:p.Thr227Ser
|
|
|
ENST00000462980.2:n.1270C>G
|
|
|
|
ENST00000472328.2:n.821C>G
|
|
|
|
ENST00000491610.2:n.715C>G
|
|
|
|
ENST00000676607.1:n.1051C>G
|
|
|
|
ENST00000676627.1:n.1485C>G
|
|
|
|
ENST00000676708.1:n.2035C>G
|
|
|
|
ENST00000676864.1:n.1904C>G
|
|
|
|
ENST00000677010.1:c.791C>G
|
ENSP00000503089.1:p.Thr264Ser
|
|
|
ENST00000677108.1:n.2661C>G
|
|
|
|
ENST00000677168.1:n.1227C>G
|
|
|
|
ENST00000677185.1:n.1318C>G
|
|
|
|
ENST00000677205.1:n.1539C>G
|
|
|
|
ENST00000677344.1:n.2029C>G
|
|
|
|
ENST00000677480.1:c.*432C>G
|
ENSP00000504378.1:n.*432C>G
|
|
|
ENST00000677519.1:n.1465C>G
|
|
|
|
ENST00000677593.1:n.1311C>G
|
|
|
|
ENST00000677740.1:n.2260C>G
|
|
|
|
ENST00000677991.1:n.1928C>G
|
|
|
|
ENST00000678001.1:n.1248C>G
|
|
|
|
ENST00000678085.1:n.1311C>G
|
|
|
|
ENST00000678177.1:n.2604C>G
|
|
|
|
ENST00000678603.1:n.1833C>G
|
|
|
|
ENST00000678724.1:c.680C>G
|
ENSP00000503874.1:p.Thr227Ser
|
|
|
ENST00000678920.1:n.913C>G
|
|
|
|
ENST00000679019.1:n.1525C>G
|
|
|
|
ENST00000679117.1:c.*570C>G
|
ENSP00000503240.1:n.*570C>G
|
|
|
ENST00000679339.1:n.1596C>G
|
|
|
|
ENST00000326739.8:c.755C>G
|
ENSP00000321584.4:p.Thr252Ser
|
|
|
ENST00000429182.5:c.549C>G
|
|
|
|
ENST00000442157.1:c.680C>G
|
ENSP00000403502.1:p.Thr227Ser
|
|
|
ENST00000462980.1:n.657C>G
|
|
|
|
ENST00000491610.1:n.715C>G
|
|
|
|
NM_000884.2:c.755C>G
|
NP_000875.2:p.Thr252Ser
|
|
|
XM_006713128.2:c.965C>G
|
XP_006713191.1:p.Thr322Ser
|
|
|
XM_006713128.3:c.965C>G
|
XP_006713191.1:p.Thr322Ser
|
|
|
XM_017006349.1:c.890C>G
|
XP_016861838.1:p.Thr297Ser
|
|
|
XM_017006350.1:c.890C>G
|
XP_016861839.1:p.Thr297Ser
|
|
|
NM_000884.3:c.755C>G
MANE Select
|
NP_000875.2:p.Thr252Ser
|
|
