|
ENST00000703936.1:c.2762A>C
|
ENSP00000515567.1:p.Lys921Thr
|
|
|
ENST00000703937.1:c.*1823A>C
|
ENSP00000515568.1:n.*1823A>C
|
|
|
ENST00000326739.9:c.722A>C
MANE Select
|
ENSP00000321584.4:p.Lys241Thr
|
|
|
ENST00000429182.6:c.722A>C
|
ENSP00000393525.2:p.Lys241Thr
|
|
|
ENST00000442157.2:c.647A>C
|
ENSP00000403502.2:p.Lys216Thr
|
|
|
ENST00000462980.2:n.1237A>C
|
|
|
|
ENST00000472328.2:n.788A>C
|
|
|
|
ENST00000491610.2:n.682A>C
|
|
|
|
ENST00000676607.1:n.1018A>C
|
|
|
|
ENST00000676627.1:n.1452A>C
|
|
|
|
ENST00000676708.1:n.2002A>C
|
|
|
|
ENST00000676864.1:n.1871A>C
|
|
|
|
ENST00000677010.1:c.758A>C
|
ENSP00000503089.1:p.Lys253Thr
|
|
|
ENST00000677108.1:n.2628A>C
|
|
|
|
ENST00000677168.1:n.1194A>C
|
|
|
|
ENST00000677185.1:n.1285A>C
|
|
|
|
ENST00000677205.1:n.1506A>C
|
|
|
|
ENST00000677344.1:n.1996A>C
|
|
|
|
ENST00000677480.1:c.*399A>C
|
ENSP00000504378.1:n.*399A>C
|
|
|
ENST00000677519.1:n.1432A>C
|
|
|
|
ENST00000677593.1:n.1278A>C
|
|
|
|
ENST00000677740.1:n.2227A>C
|
|
|
|
ENST00000677991.1:n.1895A>C
|
|
|
|
ENST00000678001.1:n.1215A>C
|
|
|
|
ENST00000678085.1:n.1278A>C
|
|
|
|
ENST00000678177.1:n.2571A>C
|
|
|
|
ENST00000678603.1:n.1800A>C
|
|
|
|
ENST00000678724.1:c.647A>C
|
ENSP00000503874.1:p.Lys216Thr
|
|
|
ENST00000678920.1:n.880A>C
|
|
|
|
ENST00000679019.1:n.1492A>C
|
|
|
|
ENST00000679117.1:c.*537A>C
|
ENSP00000503240.1:n.*537A>C
|
|
|
ENST00000679339.1:n.1563A>C
|
|
|
|
ENST00000326739.8:c.722A>C
|
ENSP00000321584.4:p.Lys241Thr
|
|
|
ENST00000429182.5:c.516A>C
|
|
|
|
ENST00000442157.1:c.647A>C
|
ENSP00000403502.1:p.Lys216Thr
|
|
|
ENST00000462980.1:n.624A>C
|
|
|
|
ENST00000491610.1:n.682A>C
|
|
|
|
NM_000884.2:c.722A>C
|
NP_000875.2:p.Lys241Thr
|
|
|
XM_006713128.2:c.932A>C
|
XP_006713191.1:p.Lys311Thr
|
|
|
XM_006713128.3:c.932A>C
|
XP_006713191.1:p.Lys311Thr
|
|
|
XM_017006349.1:c.857A>C
|
XP_016861838.1:p.Lys286Thr
|
|
|
XM_017006350.1:c.857A>C
|
XP_016861839.1:p.Lys286Thr
|
|
|
NM_000884.3:c.722A>C
MANE Select
|
NP_000875.2:p.Lys241Thr
|
|
