|
ENST00000703936.1:c.2800G>C
|
ENSP00000515567.1:p.Glu934Gln
|
|
|
ENST00000703937.1:c.*1861G>C
|
ENSP00000515568.1:n.*1861G>C
|
|
|
ENST00000326739.9:c.760G>C
MANE Select
|
ENSP00000321584.4:p.Glu254Gln
|
|
|
ENST00000429182.6:c.760G>C
|
ENSP00000393525.2:p.Glu254Gln
|
|
|
ENST00000442157.2:c.685G>C
|
ENSP00000403502.2:p.Glu229Gln
|
|
|
ENST00000462980.2:n.1275G>C
|
|
|
|
ENST00000472328.2:n.826G>C
|
|
|
|
ENST00000491610.2:n.720G>C
|
|
|
|
ENST00000676607.1:n.1056G>C
|
|
|
|
ENST00000676627.1:n.1490G>C
|
|
|
|
ENST00000676708.1:n.2040G>C
|
|
|
|
ENST00000676864.1:n.1909G>C
|
|
|
|
ENST00000677010.1:c.796G>C
|
ENSP00000503089.1:p.Glu266Gln
|
|
|
ENST00000677108.1:n.2666G>C
|
|
|
|
ENST00000677168.1:n.1232G>C
|
|
|
|
ENST00000677185.1:n.1323G>C
|
|
|
|
ENST00000677205.1:n.1544G>C
|
|
|
|
ENST00000677344.1:n.2034G>C
|
|
|
|
ENST00000677480.1:c.*437G>C
|
ENSP00000504378.1:n.*437G>C
|
|
|
ENST00000677519.1:n.1470G>C
|
|
|
|
ENST00000677593.1:n.1316G>C
|
|
|
|
ENST00000677740.1:n.2265G>C
|
|
|
|
ENST00000677991.1:n.1933G>C
|
|
|
|
ENST00000678001.1:n.1253G>C
|
|
|
|
ENST00000678085.1:n.1316G>C
|
|
|
|
ENST00000678177.1:n.2609G>C
|
|
|
|
ENST00000678603.1:n.1838G>C
|
|
|
|
ENST00000678724.1:c.685G>C
|
ENSP00000503874.1:p.Glu229Gln
|
|
|
ENST00000678920.1:n.918G>C
|
|
|
|
ENST00000679019.1:n.1530G>C
|
|
|
|
ENST00000679117.1:c.*575G>C
|
ENSP00000503240.1:n.*575G>C
|
|
|
ENST00000679339.1:n.1601G>C
|
|
|
|
ENST00000326739.8:c.760G>C
|
ENSP00000321584.4:p.Glu254Gln
|
|
|
ENST00000429182.5:c.554G>C
|
|
|
|
ENST00000442157.1:c.685G>C
|
ENSP00000403502.1:p.Glu229Gln
|
|
|
ENST00000462980.1:n.662G>C
|
|
|
|
ENST00000491610.1:n.720G>C
|
|
|
|
NM_000884.2:c.760G>C
|
NP_000875.2:p.Glu254Gln
|
|
|
XM_006713128.2:c.970G>C
|
XP_006713191.1:p.Glu324Gln
|
|
|
XM_006713128.3:c.970G>C
|
XP_006713191.1:p.Glu324Gln
|
|
|
XM_017006349.1:c.895G>C
|
XP_016861838.1:p.Glu299Gln
|
|
|
XM_017006350.1:c.895G>C
|
XP_016861839.1:p.Glu299Gln
|
|
|
NM_000884.3:c.760G>C
MANE Select
|
NP_000875.2:p.Glu254Gln
|
|
