|
ENST00000703936.1:c.2656A>T
|
ENSP00000515567.1:p.Lys886Ter
|
|
|
ENST00000703937.1:c.*1717A>T
|
ENSP00000515568.1:n.*1717A>T
|
|
|
ENST00000326739.9:c.616A>T
MANE Select
|
ENSP00000321584.4:p.Lys206Ter
|
|
|
ENST00000429182.6:c.616A>T
|
ENSP00000393525.2:p.Lys206Ter
|
|
|
ENST00000442157.2:c.541A>T
|
ENSP00000403502.2:p.Lys181Ter
|
|
|
ENST00000462980.2:n.1131A>T
|
|
|
|
ENST00000472328.2:n.682A>T
|
|
|
|
ENST00000491610.2:n.503A>T
|
|
|
|
ENST00000676607.1:n.912A>T
|
|
|
|
ENST00000676627.1:n.1346A>T
|
|
|
|
ENST00000676708.1:n.1823A>T
|
|
|
|
ENST00000676864.1:n.1692A>T
|
|
|
|
ENST00000677010.1:c.652A>T
|
ENSP00000503089.1:p.Lys218Ter
|
|
|
ENST00000677108.1:n.2449A>T
|
|
|
|
ENST00000677168.1:n.1088A>T
|
|
|
|
ENST00000677185.1:n.1106A>T
|
|
|
|
ENST00000677205.1:n.1327A>T
|
|
|
|
ENST00000677344.1:n.1817A>T
|
|
|
|
ENST00000677480.1:c.*293A>T
|
ENSP00000504378.1:n.*293A>T
|
|
|
ENST00000677519.1:n.1326A>T
|
|
|
|
ENST00000677593.1:n.1099A>T
|
|
|
|
ENST00000677740.1:n.2048A>T
|
|
|
|
ENST00000677991.1:n.1789A>T
|
|
|
|
ENST00000678001.1:n.1109A>T
|
|
|
|
ENST00000678085.1:n.1099A>T
|
|
|
|
ENST00000678177.1:n.2392A>T
|
|
|
|
ENST00000678603.1:n.1694A>T
|
|
|
|
ENST00000678724.1:c.541A>T
|
ENSP00000503874.1:p.Lys181Ter
|
|
|
ENST00000678920.1:n.774A>T
|
|
|
|
ENST00000679019.1:n.1313A>T
|
|
|
|
ENST00000679117.1:c.*431A>T
|
ENSP00000503240.1:n.*431A>T
|
|
|
ENST00000679339.1:n.1384A>T
|
|
|
|
ENST00000326739.8:c.616A>T
|
ENSP00000321584.4:p.Lys206Ter
|
|
|
ENST00000429182.5:c.410A>T
|
|
|
|
ENST00000442157.1:c.541A>T
|
ENSP00000403502.1:p.Lys181Ter
|
|
|
ENST00000462980.1:n.518A>T
|
|
|
|
ENST00000491610.1:n.503A>T
|
|
|
|
NM_000884.2:c.616A>T
|
NP_000875.2:p.Lys206Ter
|
|
|
XM_006713128.2:c.826A>T
|
XP_006713191.1:p.Lys276Ter
|
|
|
XM_006713128.3:c.826A>T
|
XP_006713191.1:p.Lys276Ter
|
|
|
XM_017006349.1:c.751A>T
|
XP_016861838.1:p.Lys251Ter
|
|
|
XM_017006350.1:c.751A>T
|
XP_016861839.1:p.Lys251Ter
|
|
|
NM_000884.3:c.616A>T
MANE Select
|
NP_000875.2:p.Lys206Ter
|
|
