|
ENST00000703936.1:c.2780G>A
|
ENSP00000515567.1:p.Gly927Glu
|
|
|
ENST00000703937.1:c.*1841G>A
|
ENSP00000515568.1:n.*1841G>A
|
|
|
ENST00000326739.9:c.740G>A
MANE Select
|
ENSP00000321584.4:p.Gly247Glu
|
|
|
ENST00000429182.6:c.740G>A
|
ENSP00000393525.2:p.Gly247Glu
|
|
|
ENST00000442157.2:c.665G>A
|
ENSP00000403502.2:p.Gly222Glu
|
|
|
ENST00000462980.2:n.1255G>A
|
|
|
|
ENST00000472328.2:n.806G>A
|
|
|
|
ENST00000491610.2:n.700G>A
|
|
|
|
ENST00000676607.1:n.1036G>A
|
|
|
|
ENST00000676627.1:n.1470G>A
|
|
|
|
ENST00000676708.1:n.2020G>A
|
|
|
|
ENST00000676864.1:n.1889G>A
|
|
|
|
ENST00000677010.1:c.776G>A
|
ENSP00000503089.1:p.Gly259Glu
|
|
|
ENST00000677108.1:n.2646G>A
|
|
|
|
ENST00000677168.1:n.1212G>A
|
|
|
|
ENST00000677185.1:n.1303G>A
|
|
|
|
ENST00000677205.1:n.1524G>A
|
|
|
|
ENST00000677344.1:n.2014G>A
|
|
|
|
ENST00000677480.1:c.*417G>A
|
ENSP00000504378.1:n.*417G>A
|
|
|
ENST00000677519.1:n.1450G>A
|
|
|
|
ENST00000677593.1:n.1296G>A
|
|
|
|
ENST00000677740.1:n.2245G>A
|
|
|
|
ENST00000677991.1:n.1913G>A
|
|
|
|
ENST00000678001.1:n.1233G>A
|
|
|
|
ENST00000678085.1:n.1296G>A
|
|
|
|
ENST00000678177.1:n.2589G>A
|
|
|
|
ENST00000678603.1:n.1818G>A
|
|
|
|
ENST00000678724.1:c.665G>A
|
ENSP00000503874.1:p.Gly222Glu
|
|
|
ENST00000678920.1:n.898G>A
|
|
|
|
ENST00000679019.1:n.1510G>A
|
|
|
|
ENST00000679117.1:c.*555G>A
|
ENSP00000503240.1:n.*555G>A
|
|
|
ENST00000679339.1:n.1581G>A
|
|
|
|
ENST00000326739.8:c.740G>A
|
ENSP00000321584.4:p.Gly247Glu
|
|
|
ENST00000429182.5:c.534G>A
|
|
|
|
ENST00000442157.1:c.665G>A
|
ENSP00000403502.1:p.Gly222Glu
|
|
|
ENST00000462980.1:n.642G>A
|
|
|
|
ENST00000491610.1:n.700G>A
|
|
|
|
NM_000884.2:c.740G>A
|
NP_000875.2:p.Gly247Glu
|
|
|
XM_006713128.2:c.950G>A
|
XP_006713191.1:p.Gly317Glu
|
|
|
XM_006713128.3:c.950G>A
|
XP_006713191.1:p.Gly317Glu
|
|
|
XM_017006349.1:c.875G>A
|
XP_016861838.1:p.Gly292Glu
|
|
|
XM_017006350.1:c.875G>A
|
XP_016861839.1:p.Gly292Glu
|
|
|
NM_000884.3:c.740G>A
MANE Select
|
NP_000875.2:p.Gly247Glu
|
|
