|
ENST00000703936.1:c.2873G>C
|
ENSP00000515567.1:p.Gly958Ala
|
|
|
ENST00000703937.1:c.*1934G>C
|
ENSP00000515568.1:n.*1934G>C
|
|
|
ENST00000326739.9:c.833G>C
MANE Select
|
ENSP00000321584.4:p.Gly278Ala
|
|
|
ENST00000429182.6:c.833G>C
|
ENSP00000393525.2:p.Gly278Ala
|
|
|
ENST00000442157.2:c.758G>C
|
ENSP00000403502.2:p.Gly253Ala
|
|
|
ENST00000462980.2:n.1348G>C
|
|
|
|
ENST00000472328.2:n.899G>C
|
|
|
|
ENST00000491610.2:n.793G>C
|
|
|
|
ENST00000676607.1:n.1129G>C
|
|
|
|
ENST00000676627.1:n.1563G>C
|
|
|
|
ENST00000676708.1:n.2113G>C
|
|
|
|
ENST00000676864.1:n.1982G>C
|
|
|
|
ENST00000677010.1:c.857G>C
|
ENSP00000503089.1:p.Gly286Ala
|
|
|
ENST00000677108.1:n.2816G>C
|
|
|
|
ENST00000677168.1:n.1305G>C
|
|
|
|
ENST00000677185.1:n.1396G>C
|
|
|
|
ENST00000677205.1:n.1617G>C
|
|
|
|
ENST00000677344.1:n.2107G>C
|
|
|
|
ENST00000677480.1:c.*510G>C
|
ENSP00000504378.1:n.*510G>C
|
|
|
ENST00000677519.1:n.1543G>C
|
|
|
|
ENST00000677593.1:n.1389G>C
|
|
|
|
ENST00000677740.1:n.2338G>C
|
|
|
|
ENST00000677991.1:n.2006G>C
|
|
|
|
ENST00000678001.1:n.1326G>C
|
|
|
|
ENST00000678085.1:n.1466G>C
|
|
|
|
ENST00000678177.1:n.2759G>C
|
|
|
|
ENST00000678603.1:n.1911G>C
|
|
|
|
ENST00000678724.1:c.758G>C
|
ENSP00000503874.1:p.Gly253Ala
|
|
|
ENST00000678920.1:n.991G>C
|
|
|
|
ENST00000679019.1:n.1680G>C
|
|
|
|
ENST00000679117.1:c.*648G>C
|
ENSP00000503240.1:n.*648G>C
|
|
|
ENST00000679339.1:n.1674G>C
|
|
|
|
ENST00000326739.8:c.833G>C
|
ENSP00000321584.4:p.Gly278Ala
|
|
|
ENST00000429182.5:c.627G>C
|
|
|
|
ENST00000442157.1:c.758G>C
|
ENSP00000403502.1:p.Gly253Ala
|
|
|
ENST00000462980.1:n.735G>C
|
|
|
|
ENST00000491610.1:n.793G>C
|
|
|
|
NM_000884.2:c.833G>C
|
NP_000875.2:p.Gly278Ala
|
|
|
XM_006713128.2:c.1043G>C
|
XP_006713191.1:p.Gly348Ala
|
|
|
XM_006713128.3:c.1043G>C
|
XP_006713191.1:p.Gly348Ala
|
|
|
XM_017006349.1:c.968G>C
|
XP_016861838.1:p.Gly323Ala
|
|
|
XM_017006350.1:c.968G>C
|
XP_016861839.1:p.Gly323Ala
|
|
|
NM_000884.3:c.833G>C
MANE Select
|
NP_000875.2:p.Gly278Ala
|
|
