|
ENST00000703936.1:c.2791G>A
|
ENSP00000515567.1:p.Gly931Ser
|
|
|
ENST00000703937.1:c.*1852G>A
|
ENSP00000515568.1:n.*1852G>A
|
|
|
ENST00000326739.9:c.751G>A
MANE Select
|
ENSP00000321584.4:p.Gly251Ser
|
|
|
ENST00000429182.6:c.751G>A
|
ENSP00000393525.2:p.Gly251Ser
|
|
|
ENST00000442157.2:c.676G>A
|
ENSP00000403502.2:p.Gly226Ser
|
|
|
ENST00000462980.2:n.1266G>A
|
|
|
|
ENST00000472328.2:n.817G>A
|
|
|
|
ENST00000491610.2:n.711G>A
|
|
|
|
ENST00000676607.1:n.1047G>A
|
|
|
|
ENST00000676627.1:n.1481G>A
|
|
|
|
ENST00000676708.1:n.2031G>A
|
|
|
|
ENST00000676864.1:n.1900G>A
|
|
|
|
ENST00000677010.1:c.787G>A
|
ENSP00000503089.1:p.Gly263Ser
|
|
|
ENST00000677108.1:n.2657G>A
|
|
|
|
ENST00000677168.1:n.1223G>A
|
|
|
|
ENST00000677185.1:n.1314G>A
|
|
|
|
ENST00000677205.1:n.1535G>A
|
|
|
|
ENST00000677344.1:n.2025G>A
|
|
|
|
ENST00000677480.1:c.*428G>A
|
ENSP00000504378.1:n.*428G>A
|
|
|
ENST00000677519.1:n.1461G>A
|
|
|
|
ENST00000677593.1:n.1307G>A
|
|
|
|
ENST00000677740.1:n.2256G>A
|
|
|
|
ENST00000677991.1:n.1924G>A
|
|
|
|
ENST00000678001.1:n.1244G>A
|
|
|
|
ENST00000678085.1:n.1307G>A
|
|
|
|
ENST00000678177.1:n.2600G>A
|
|
|
|
ENST00000678603.1:n.1829G>A
|
|
|
|
ENST00000678724.1:c.676G>A
|
ENSP00000503874.1:p.Gly226Ser
|
|
|
ENST00000678920.1:n.909G>A
|
|
|
|
ENST00000679019.1:n.1521G>A
|
|
|
|
ENST00000679117.1:c.*566G>A
|
ENSP00000503240.1:n.*566G>A
|
|
|
ENST00000679339.1:n.1592G>A
|
|
|
|
ENST00000326739.8:c.751G>A
|
ENSP00000321584.4:p.Gly251Ser
|
|
|
ENST00000429182.5:c.545G>A
|
|
|
|
ENST00000442157.1:c.676G>A
|
ENSP00000403502.1:p.Gly226Ser
|
|
|
ENST00000462980.1:n.653G>A
|
|
|
|
ENST00000491610.1:n.711G>A
|
|
|
|
NM_000884.2:c.751G>A
|
NP_000875.2:p.Gly251Ser
|
|
|
XM_006713128.2:c.961G>A
|
XP_006713191.1:p.Gly321Ser
|
|
|
XM_006713128.3:c.961G>A
|
XP_006713191.1:p.Gly321Ser
|
|
|
XM_017006349.1:c.886G>A
|
XP_016861838.1:p.Gly296Ser
|
|
|
XM_017006350.1:c.886G>A
|
XP_016861839.1:p.Gly296Ser
|
|
|
NM_000884.3:c.751G>A
MANE Select
|
NP_000875.2:p.Gly251Ser
|
|
