|
ENST00000703936.1:c.2650A>G
|
ENSP00000515567.1:p.Ser884Gly
|
|
|
ENST00000703937.1:c.*1711A>G
|
ENSP00000515568.1:n.*1711A>G
|
|
|
ENST00000326739.9:c.610A>G
MANE Select
|
ENSP00000321584.4:p.Ser204Gly
|
|
|
ENST00000429182.6:c.610A>G
|
ENSP00000393525.2:p.Ser204Gly
|
|
|
ENST00000442157.2:c.535A>G
|
ENSP00000403502.2:p.Ser179Gly
|
|
|
ENST00000462980.2:n.1125A>G
|
|
|
|
ENST00000472328.2:n.676A>G
|
|
|
|
ENST00000491610.2:n.497A>G
|
|
|
|
ENST00000676607.1:n.906A>G
|
|
|
|
ENST00000676627.1:n.1340A>G
|
|
|
|
ENST00000676708.1:n.1817A>G
|
|
|
|
ENST00000676864.1:n.1686A>G
|
|
|
|
ENST00000677010.1:c.646A>G
|
ENSP00000503089.1:p.Ser216Gly
|
|
|
ENST00000677108.1:n.2443A>G
|
|
|
|
ENST00000677168.1:n.1082A>G
|
|
|
|
ENST00000677185.1:n.1100A>G
|
|
|
|
ENST00000677205.1:n.1321A>G
|
|
|
|
ENST00000677344.1:n.1811A>G
|
|
|
|
ENST00000677480.1:c.*287A>G
|
ENSP00000504378.1:n.*287A>G
|
|
|
ENST00000677519.1:n.1320A>G
|
|
|
|
ENST00000677593.1:n.1093A>G
|
|
|
|
ENST00000677740.1:n.2042A>G
|
|
|
|
ENST00000677991.1:n.1783A>G
|
|
|
|
ENST00000678001.1:n.1103A>G
|
|
|
|
ENST00000678085.1:n.1093A>G
|
|
|
|
ENST00000678177.1:n.2386A>G
|
|
|
|
ENST00000678603.1:n.1688A>G
|
|
|
|
ENST00000678724.1:c.535A>G
|
ENSP00000503874.1:p.Ser179Gly
|
|
|
ENST00000678920.1:n.768A>G
|
|
|
|
ENST00000679019.1:n.1307A>G
|
|
|
|
ENST00000679117.1:c.*425A>G
|
ENSP00000503240.1:n.*425A>G
|
|
|
ENST00000679339.1:n.1378A>G
|
|
|
|
ENST00000326739.8:c.610A>G
|
ENSP00000321584.4:p.Ser204Gly
|
|
|
ENST00000429182.5:c.404A>G
|
|
|
|
ENST00000442157.1:c.535A>G
|
ENSP00000403502.1:p.Ser179Gly
|
|
|
ENST00000462980.1:n.512A>G
|
|
|
|
ENST00000491610.1:n.497A>G
|
|
|
|
NM_000884.2:c.610A>G
|
NP_000875.2:p.Ser204Gly
|
|
|
XM_006713128.2:c.820A>G
|
XP_006713191.1:p.Ser274Gly
|
|
|
XM_006713128.3:c.820A>G
|
XP_006713191.1:p.Ser274Gly
|
|
|
XM_017006349.1:c.745A>G
|
XP_016861838.1:p.Ser249Gly
|
|
|
XM_017006350.1:c.745A>G
|
XP_016861839.1:p.Ser249Gly
|
|
|
NM_000884.3:c.610A>G
MANE Select
|
NP_000875.2:p.Ser204Gly
|
|
