|
ENST00000703936.1:c.2782G>A
|
ENSP00000515567.1:p.Ala928Thr
|
|
|
ENST00000703937.1:c.*1843G>A
|
ENSP00000515568.1:n.*1843G>A
|
|
|
ENST00000326739.9:c.742G>A
MANE Select
|
ENSP00000321584.4:p.Ala248Thr
|
|
|
ENST00000429182.6:c.742G>A
|
ENSP00000393525.2:p.Ala248Thr
|
|
|
ENST00000442157.2:c.667G>A
|
ENSP00000403502.2:p.Ala223Thr
|
|
|
ENST00000462980.2:n.1257G>A
|
|
|
|
ENST00000472328.2:n.808G>A
|
|
|
|
ENST00000491610.2:n.702G>A
|
|
|
|
ENST00000676607.1:n.1038G>A
|
|
|
|
ENST00000676627.1:n.1472G>A
|
|
|
|
ENST00000676708.1:n.2022G>A
|
|
|
|
ENST00000676864.1:n.1891G>A
|
|
|
|
ENST00000677010.1:c.778G>A
|
ENSP00000503089.1:p.Ala260Thr
|
|
|
ENST00000677108.1:n.2648G>A
|
|
|
|
ENST00000677168.1:n.1214G>A
|
|
|
|
ENST00000677185.1:n.1305G>A
|
|
|
|
ENST00000677205.1:n.1526G>A
|
|
|
|
ENST00000677344.1:n.2016G>A
|
|
|
|
ENST00000677480.1:c.*419G>A
|
ENSP00000504378.1:n.*419G>A
|
|
|
ENST00000677519.1:n.1452G>A
|
|
|
|
ENST00000677593.1:n.1298G>A
|
|
|
|
ENST00000677740.1:n.2247G>A
|
|
|
|
ENST00000677991.1:n.1915G>A
|
|
|
|
ENST00000678001.1:n.1235G>A
|
|
|
|
ENST00000678085.1:n.1298G>A
|
|
|
|
ENST00000678177.1:n.2591G>A
|
|
|
|
ENST00000678603.1:n.1820G>A
|
|
|
|
ENST00000678724.1:c.667G>A
|
ENSP00000503874.1:p.Ala223Thr
|
|
|
ENST00000678920.1:n.900G>A
|
|
|
|
ENST00000679019.1:n.1512G>A
|
|
|
|
ENST00000679117.1:c.*557G>A
|
ENSP00000503240.1:n.*557G>A
|
|
|
ENST00000679339.1:n.1583G>A
|
|
|
|
ENST00000326739.8:c.742G>A
|
ENSP00000321584.4:p.Ala248Thr
|
|
|
ENST00000429182.5:c.536G>A
|
|
|
|
ENST00000442157.1:c.667G>A
|
ENSP00000403502.1:p.Ala223Thr
|
|
|
ENST00000462980.1:n.644G>A
|
|
|
|
ENST00000491610.1:n.702G>A
|
|
|
|
NM_000884.2:c.742G>A
|
NP_000875.2:p.Ala248Thr
|
|
|
XM_006713128.2:c.952G>A
|
XP_006713191.1:p.Ala318Thr
|
|
|
XM_006713128.3:c.952G>A
|
XP_006713191.1:p.Ala318Thr
|
|
|
XM_017006349.1:c.877G>A
|
XP_016861838.1:p.Ala293Thr
|
|
|
XM_017006350.1:c.877G>A
|
XP_016861839.1:p.Ala293Thr
|
|
|
NM_000884.3:c.742G>A
MANE Select
|
NP_000875.2:p.Ala248Thr
|
|
