|
ENST00000703936.1:c.2635G>C
|
ENSP00000515567.1:p.Glu879Gln
|
|
|
ENST00000703937.1:c.*1696G>C
|
ENSP00000515568.1:n.*1696G>C
|
|
|
ENST00000326739.9:c.595G>C
MANE Select
|
ENSP00000321584.4:p.Glu199Gln
|
|
|
ENST00000429182.6:c.595G>C
|
ENSP00000393525.2:p.Glu199Gln
|
|
|
ENST00000442157.2:c.520G>C
|
ENSP00000403502.2:p.Glu174Gln
|
|
|
ENST00000462980.2:n.1110G>C
|
|
|
|
ENST00000472328.2:n.661G>C
|
|
|
|
ENST00000491610.2:n.482G>C
|
|
|
|
ENST00000676607.1:n.891G>C
|
|
|
|
ENST00000676627.1:n.1325G>C
|
|
|
|
ENST00000676708.1:n.1802G>C
|
|
|
|
ENST00000676864.1:n.1671G>C
|
|
|
|
ENST00000677010.1:c.631G>C
|
ENSP00000503089.1:p.Glu211Gln
|
|
|
ENST00000677108.1:n.2428G>C
|
|
|
|
ENST00000677168.1:n.1067G>C
|
|
|
|
ENST00000677185.1:n.1085G>C
|
|
|
|
ENST00000677205.1:n.1306G>C
|
|
|
|
ENST00000677344.1:n.1796G>C
|
|
|
|
ENST00000677480.1:c.*272G>C
|
ENSP00000504378.1:n.*272G>C
|
|
|
ENST00000677519.1:n.1305G>C
|
|
|
|
ENST00000677593.1:n.1078G>C
|
|
|
|
ENST00000677740.1:n.2027G>C
|
|
|
|
ENST00000677991.1:n.1768G>C
|
|
|
|
ENST00000678001.1:n.1088G>C
|
|
|
|
ENST00000678085.1:n.1078G>C
|
|
|
|
ENST00000678177.1:n.2371G>C
|
|
|
|
ENST00000678603.1:n.1673G>C
|
|
|
|
ENST00000678724.1:c.520G>C
|
ENSP00000503874.1:p.Glu174Gln
|
|
|
ENST00000678920.1:n.753G>C
|
|
|
|
ENST00000679019.1:n.1292G>C
|
|
|
|
ENST00000679117.1:c.*410G>C
|
ENSP00000503240.1:n.*410G>C
|
|
|
ENST00000679339.1:n.1363G>C
|
|
|
|
ENST00000326739.8:c.595G>C
|
ENSP00000321584.4:p.Glu199Gln
|
|
|
ENST00000429182.5:c.389G>C
|
|
|
|
ENST00000442157.1:c.520G>C
|
ENSP00000403502.1:p.Glu174Gln
|
|
|
ENST00000462980.1:n.497G>C
|
|
|
|
ENST00000491610.1:n.482G>C
|
|
|
|
NM_000884.2:c.595G>C
|
NP_000875.2:p.Glu199Gln
|
|
|
XM_006713128.2:c.805G>C
|
XP_006713191.1:p.Glu269Gln
|
|
|
XM_006713128.3:c.805G>C
|
XP_006713191.1:p.Glu269Gln
|
|
|
XM_017006349.1:c.730G>C
|
XP_016861838.1:p.Glu244Gln
|
|
|
XM_017006350.1:c.730G>C
|
XP_016861839.1:p.Glu244Gln
|
|
|
NM_000884.3:c.595G>C
MANE Select
|
NP_000875.2:p.Glu199Gln
|
|
