|
ENST00000703936.1:c.2731C>G
|
ENSP00000515567.1:p.Arg911Gly
|
|
|
ENST00000703937.1:c.*1792C>G
|
ENSP00000515568.1:n.*1792C>G
|
|
|
ENST00000326739.9:c.691C>G
MANE Select
|
ENSP00000321584.4:p.Arg231Gly
|
|
|
ENST00000429182.6:c.691C>G
|
ENSP00000393525.2:p.Arg231Gly
|
|
|
ENST00000442157.2:c.616C>G
|
ENSP00000403502.2:p.Arg206Gly
|
|
|
ENST00000462980.2:n.1206C>G
|
|
|
|
ENST00000472328.2:n.757C>G
|
|
|
|
ENST00000491610.2:n.651C>G
|
|
|
|
ENST00000676607.1:n.987C>G
|
|
|
|
ENST00000676627.1:n.1421C>G
|
|
|
|
ENST00000676708.1:n.1971C>G
|
|
|
|
ENST00000676864.1:n.1840C>G
|
|
|
|
ENST00000677010.1:c.727C>G
|
ENSP00000503089.1:p.Arg243Gly
|
|
|
ENST00000677108.1:n.2597C>G
|
|
|
|
ENST00000677168.1:n.1163C>G
|
|
|
|
ENST00000677185.1:n.1254C>G
|
|
|
|
ENST00000677205.1:n.1475C>G
|
|
|
|
ENST00000677344.1:n.1965C>G
|
|
|
|
ENST00000677480.1:c.*368C>G
|
ENSP00000504378.1:n.*368C>G
|
|
|
ENST00000677519.1:n.1401C>G
|
|
|
|
ENST00000677593.1:n.1247C>G
|
|
|
|
ENST00000677740.1:n.2196C>G
|
|
|
|
ENST00000677991.1:n.1864C>G
|
|
|
|
ENST00000678001.1:n.1184C>G
|
|
|
|
ENST00000678085.1:n.1247C>G
|
|
|
|
ENST00000678177.1:n.2540C>G
|
|
|
|
ENST00000678603.1:n.1769C>G
|
|
|
|
ENST00000678724.1:c.616C>G
|
ENSP00000503874.1:p.Arg206Gly
|
|
|
ENST00000678920.1:n.849C>G
|
|
|
|
ENST00000679019.1:n.1461C>G
|
|
|
|
ENST00000679117.1:c.*506C>G
|
ENSP00000503240.1:n.*506C>G
|
|
|
ENST00000679339.1:n.1532C>G
|
|
|
|
ENST00000326739.8:c.691C>G
|
ENSP00000321584.4:p.Arg231Gly
|
|
|
ENST00000429182.5:c.485C>G
|
|
|
|
ENST00000442157.1:c.616C>G
|
ENSP00000403502.1:p.Arg206Gly
|
|
|
ENST00000462980.1:n.593C>G
|
|
|
|
ENST00000491610.1:n.651C>G
|
|
|
|
NM_000884.2:c.691C>G
|
NP_000875.2:p.Arg231Gly
|
|
|
XM_006713128.2:c.901C>G
|
XP_006713191.1:p.Arg301Gly
|
|
|
XM_006713128.3:c.901C>G
|
XP_006713191.1:p.Arg301Gly
|
|
|
XM_017006349.1:c.826C>G
|
XP_016861838.1:p.Arg276Gly
|
|
|
XM_017006350.1:c.826C>G
|
XP_016861839.1:p.Arg276Gly
|
|
|
NM_000884.3:c.691C>G
MANE Select
|
NP_000875.2:p.Arg231Gly
|
|
