|
ENST00000703936.1:c.2698G>T
|
ENSP00000515567.1:p.Ala900Ser
|
|
|
ENST00000703937.1:c.*1759G>T
|
ENSP00000515568.1:n.*1759G>T
|
|
|
ENST00000326739.9:c.658G>T
MANE Select
|
ENSP00000321584.4:p.Ala220Ser
|
|
|
ENST00000429182.6:c.658G>T
|
ENSP00000393525.2:p.Ala220Ser
|
|
|
ENST00000442157.2:c.583G>T
|
ENSP00000403502.2:p.Ala195Ser
|
|
|
ENST00000462980.2:n.1173G>T
|
|
|
|
ENST00000472328.2:n.724G>T
|
|
|
|
ENST00000491610.2:n.618G>T
|
|
|
|
ENST00000676607.1:n.954G>T
|
|
|
|
ENST00000676627.1:n.1388G>T
|
|
|
|
ENST00000676708.1:n.1938G>T
|
|
|
|
ENST00000676864.1:n.1807G>T
|
|
|
|
ENST00000677010.1:c.694G>T
|
ENSP00000503089.1:p.Ala232Ser
|
|
|
ENST00000677108.1:n.2564G>T
|
|
|
|
ENST00000677168.1:n.1130G>T
|
|
|
|
ENST00000677185.1:n.1221G>T
|
|
|
|
ENST00000677205.1:n.1442G>T
|
|
|
|
ENST00000677344.1:n.1932G>T
|
|
|
|
ENST00000677480.1:c.*335G>T
|
ENSP00000504378.1:n.*335G>T
|
|
|
ENST00000677519.1:n.1368G>T
|
|
|
|
ENST00000677593.1:n.1214G>T
|
|
|
|
ENST00000677740.1:n.2163G>T
|
|
|
|
ENST00000677991.1:n.1831G>T
|
|
|
|
ENST00000678001.1:n.1151G>T
|
|
|
|
ENST00000678085.1:n.1214G>T
|
|
|
|
ENST00000678177.1:n.2507G>T
|
|
|
|
ENST00000678603.1:n.1736G>T
|
|
|
|
ENST00000678724.1:c.583G>T
|
ENSP00000503874.1:p.Ala195Ser
|
|
|
ENST00000678920.1:n.816G>T
|
|
|
|
ENST00000679019.1:n.1428G>T
|
|
|
|
ENST00000679117.1:c.*473G>T
|
ENSP00000503240.1:n.*473G>T
|
|
|
ENST00000679339.1:n.1499G>T
|
|
|
|
ENST00000326739.8:c.658G>T
|
ENSP00000321584.4:p.Ala220Ser
|
|
|
ENST00000429182.5:c.452G>T
|
|
|
|
ENST00000442157.1:c.583G>T
|
ENSP00000403502.1:p.Ala195Ser
|
|
|
ENST00000462980.1:n.560G>T
|
|
|
|
ENST00000491610.1:n.618G>T
|
|
|
|
NM_000884.2:c.658G>T
|
NP_000875.2:p.Ala220Ser
|
|
|
XM_006713128.2:c.868G>T
|
XP_006713191.1:p.Ala290Ser
|
|
|
XM_006713128.3:c.868G>T
|
XP_006713191.1:p.Ala290Ser
|
|
|
XM_017006349.1:c.793G>T
|
XP_016861838.1:p.Ala265Ser
|
|
|
XM_017006350.1:c.793G>T
|
XP_016861839.1:p.Ala265Ser
|
|
|
NM_000884.3:c.658G>T
MANE Select
|
NP_000875.2:p.Ala220Ser
|
|
