|
ENST00000703936.1:c.2666T>C
|
ENSP00000515567.1:p.Leu889Ser
|
|
|
ENST00000703937.1:c.*1727T>C
|
ENSP00000515568.1:n.*1727T>C
|
|
|
ENST00000326739.9:c.626T>C
MANE Select
|
ENSP00000321584.4:p.Leu209Ser
|
|
|
ENST00000429182.6:c.626T>C
|
ENSP00000393525.2:p.Leu209Ser
|
|
|
ENST00000442157.2:c.551T>C
|
ENSP00000403502.2:p.Leu184Ser
|
|
|
ENST00000462980.2:n.1141T>C
|
|
|
|
ENST00000472328.2:n.692T>C
|
|
|
|
ENST00000491610.2:n.586T>C
|
|
|
|
ENST00000676607.1:n.922T>C
|
|
|
|
ENST00000676627.1:n.1356T>C
|
|
|
|
ENST00000676708.1:n.1906T>C
|
|
|
|
ENST00000676864.1:n.1775T>C
|
|
|
|
ENST00000677010.1:c.662T>C
|
ENSP00000503089.1:p.Leu221Ser
|
|
|
ENST00000677108.1:n.2532T>C
|
|
|
|
ENST00000677168.1:n.1098T>C
|
|
|
|
ENST00000677185.1:n.1189T>C
|
|
|
|
ENST00000677205.1:n.1410T>C
|
|
|
|
ENST00000677344.1:n.1900T>C
|
|
|
|
ENST00000677480.1:c.*303T>C
|
ENSP00000504378.1:n.*303T>C
|
|
|
ENST00000677519.1:n.1336T>C
|
|
|
|
ENST00000677593.1:n.1182T>C
|
|
|
|
ENST00000677740.1:n.2131T>C
|
|
|
|
ENST00000677991.1:n.1799T>C
|
|
|
|
ENST00000678001.1:n.1119T>C
|
|
|
|
ENST00000678085.1:n.1182T>C
|
|
|
|
ENST00000678177.1:n.2475T>C
|
|
|
|
ENST00000678603.1:n.1704T>C
|
|
|
|
ENST00000678724.1:c.551T>C
|
ENSP00000503874.1:p.Leu184Ser
|
|
|
ENST00000678920.1:n.784T>C
|
|
|
|
ENST00000679019.1:n.1396T>C
|
|
|
|
ENST00000679117.1:c.*441T>C
|
ENSP00000503240.1:n.*441T>C
|
|
|
ENST00000679339.1:n.1467T>C
|
|
|
|
ENST00000326739.8:c.626T>C
|
ENSP00000321584.4:p.Leu209Ser
|
|
|
ENST00000429182.5:c.420T>C
|
|
|
|
ENST00000442157.1:c.551T>C
|
ENSP00000403502.1:p.Leu184Ser
|
|
|
ENST00000462980.1:n.528T>C
|
|
|
|
ENST00000491610.1:n.586T>C
|
|
|
|
NM_000884.2:c.626T>C
|
NP_000875.2:p.Leu209Ser
|
|
|
XM_006713128.2:c.836T>C
|
XP_006713191.1:p.Leu279Ser
|
|
|
XM_006713128.3:c.836T>C
|
XP_006713191.1:p.Leu279Ser
|
|
|
XM_017006349.1:c.761T>C
|
XP_016861838.1:p.Leu254Ser
|
|
|
XM_017006350.1:c.761T>C
|
XP_016861839.1:p.Leu254Ser
|
|
|
NM_000884.3:c.626T>C
MANE Select
|
NP_000875.2:p.Leu209Ser
|
|
