|
ENST00000703936.1:c.2689G>C
|
ENSP00000515567.1:p.Glu897Gln
|
|
|
ENST00000703937.1:c.*1750G>C
|
ENSP00000515568.1:n.*1750G>C
|
|
|
ENST00000326739.9:c.649G>C
MANE Select
|
ENSP00000321584.4:p.Glu217Gln
|
|
|
ENST00000429182.6:c.649G>C
|
ENSP00000393525.2:p.Glu217Gln
|
|
|
ENST00000442157.2:c.574G>C
|
ENSP00000403502.2:p.Glu192Gln
|
|
|
ENST00000462980.2:n.1164G>C
|
|
|
|
ENST00000472328.2:n.715G>C
|
|
|
|
ENST00000491610.2:n.609G>C
|
|
|
|
ENST00000676607.1:n.945G>C
|
|
|
|
ENST00000676627.1:n.1379G>C
|
|
|
|
ENST00000676708.1:n.1929G>C
|
|
|
|
ENST00000676864.1:n.1798G>C
|
|
|
|
ENST00000677010.1:c.685G>C
|
ENSP00000503089.1:p.Glu229Gln
|
|
|
ENST00000677108.1:n.2555G>C
|
|
|
|
ENST00000677168.1:n.1121G>C
|
|
|
|
ENST00000677185.1:n.1212G>C
|
|
|
|
ENST00000677205.1:n.1433G>C
|
|
|
|
ENST00000677344.1:n.1923G>C
|
|
|
|
ENST00000677480.1:c.*326G>C
|
ENSP00000504378.1:n.*326G>C
|
|
|
ENST00000677519.1:n.1359G>C
|
|
|
|
ENST00000677593.1:n.1205G>C
|
|
|
|
ENST00000677740.1:n.2154G>C
|
|
|
|
ENST00000677991.1:n.1822G>C
|
|
|
|
ENST00000678001.1:n.1142G>C
|
|
|
|
ENST00000678085.1:n.1205G>C
|
|
|
|
ENST00000678177.1:n.2498G>C
|
|
|
|
ENST00000678603.1:n.1727G>C
|
|
|
|
ENST00000678724.1:c.574G>C
|
ENSP00000503874.1:p.Glu192Gln
|
|
|
ENST00000678920.1:n.807G>C
|
|
|
|
ENST00000679019.1:n.1419G>C
|
|
|
|
ENST00000679117.1:c.*464G>C
|
ENSP00000503240.1:n.*464G>C
|
|
|
ENST00000679339.1:n.1490G>C
|
|
|
|
ENST00000326739.8:c.649G>C
|
ENSP00000321584.4:p.Glu217Gln
|
|
|
ENST00000429182.5:c.443G>C
|
|
|
|
ENST00000442157.1:c.574G>C
|
ENSP00000403502.1:p.Glu192Gln
|
|
|
ENST00000462980.1:n.551G>C
|
|
|
|
ENST00000491610.1:n.609G>C
|
|
|
|
NM_000884.2:c.649G>C
|
NP_000875.2:p.Glu217Gln
|
|
|
XM_006713128.2:c.859G>C
|
XP_006713191.1:p.Glu287Gln
|
|
|
XM_006713128.3:c.859G>C
|
XP_006713191.1:p.Glu287Gln
|
|
|
XM_017006349.1:c.784G>C
|
XP_016861838.1:p.Glu262Gln
|
|
|
XM_017006350.1:c.784G>C
|
XP_016861839.1:p.Glu262Gln
|
|
|
NM_000884.3:c.649G>C
MANE Select
|
NP_000875.2:p.Glu217Gln
|
|
