|
ENST00000703936.1:c.2746G>A
|
ENSP00000515567.1:p.Ala916Thr
|
|
|
ENST00000703937.1:c.*1807G>A
|
ENSP00000515568.1:n.*1807G>A
|
|
|
ENST00000326739.9:c.706G>A
MANE Select
|
ENSP00000321584.4:p.Ala236Thr
|
|
|
ENST00000429182.6:c.706G>A
|
ENSP00000393525.2:p.Ala236Thr
|
|
|
ENST00000442157.2:c.631G>A
|
ENSP00000403502.2:p.Ala211Thr
|
|
|
ENST00000462980.2:n.1221G>A
|
|
|
|
ENST00000472328.2:n.772G>A
|
|
|
|
ENST00000491610.2:n.666G>A
|
|
|
|
ENST00000676607.1:n.1002G>A
|
|
|
|
ENST00000676627.1:n.1436G>A
|
|
|
|
ENST00000676708.1:n.1986G>A
|
|
|
|
ENST00000676864.1:n.1855G>A
|
|
|
|
ENST00000677010.1:c.742G>A
|
ENSP00000503089.1:p.Ala248Thr
|
|
|
ENST00000677108.1:n.2612G>A
|
|
|
|
ENST00000677168.1:n.1178G>A
|
|
|
|
ENST00000677185.1:n.1269G>A
|
|
|
|
ENST00000677205.1:n.1490G>A
|
|
|
|
ENST00000677344.1:n.1980G>A
|
|
|
|
ENST00000677480.1:c.*383G>A
|
ENSP00000504378.1:n.*383G>A
|
|
|
ENST00000677519.1:n.1416G>A
|
|
|
|
ENST00000677593.1:n.1262G>A
|
|
|
|
ENST00000677740.1:n.2211G>A
|
|
|
|
ENST00000677991.1:n.1879G>A
|
|
|
|
ENST00000678001.1:n.1199G>A
|
|
|
|
ENST00000678085.1:n.1262G>A
|
|
|
|
ENST00000678177.1:n.2555G>A
|
|
|
|
ENST00000678603.1:n.1784G>A
|
|
|
|
ENST00000678724.1:c.631G>A
|
ENSP00000503874.1:p.Ala211Thr
|
|
|
ENST00000678920.1:n.864G>A
|
|
|
|
ENST00000679019.1:n.1476G>A
|
|
|
|
ENST00000679117.1:c.*521G>A
|
ENSP00000503240.1:n.*521G>A
|
|
|
ENST00000679339.1:n.1547G>A
|
|
|
|
ENST00000326739.8:c.706G>A
|
ENSP00000321584.4:p.Ala236Thr
|
|
|
ENST00000429182.5:c.500G>A
|
|
|
|
ENST00000442157.1:c.631G>A
|
ENSP00000403502.1:p.Ala211Thr
|
|
|
ENST00000462980.1:n.608G>A
|
|
|
|
ENST00000491610.1:n.666G>A
|
|
|
|
NM_000884.2:c.706G>A
|
NP_000875.2:p.Ala236Thr
|
|
|
XM_006713128.2:c.916G>A
|
XP_006713191.1:p.Ala306Thr
|
|
|
XM_006713128.3:c.916G>A
|
XP_006713191.1:p.Ala306Thr
|
|
|
XM_017006349.1:c.841G>A
|
XP_016861838.1:p.Ala281Thr
|
|
|
XM_017006350.1:c.841G>A
|
XP_016861839.1:p.Ala281Thr
|
|
|
NM_000884.3:c.706G>A
MANE Select
|
NP_000875.2:p.Ala236Thr
|
|
