|
ENST00000703936.1:c.2732G>T
|
ENSP00000515567.1:p.Arg911Leu
|
|
|
ENST00000703937.1:c.*1793G>T
|
ENSP00000515568.1:n.*1793G>T
|
|
|
ENST00000326739.9:c.692G>T
MANE Select
|
ENSP00000321584.4:p.Arg231Leu
|
|
|
ENST00000429182.6:c.692G>T
|
ENSP00000393525.2:p.Arg231Leu
|
|
|
ENST00000442157.2:c.617G>T
|
ENSP00000403502.2:p.Arg206Leu
|
|
|
ENST00000462980.2:n.1207G>T
|
|
|
|
ENST00000472328.2:n.758G>T
|
|
|
|
ENST00000491610.2:n.652G>T
|
|
|
|
ENST00000676607.1:n.988G>T
|
|
|
|
ENST00000676627.1:n.1422G>T
|
|
|
|
ENST00000676708.1:n.1972G>T
|
|
|
|
ENST00000676864.1:n.1841G>T
|
|
|
|
ENST00000677010.1:c.728G>T
|
ENSP00000503089.1:p.Arg243Leu
|
|
|
ENST00000677108.1:n.2598G>T
|
|
|
|
ENST00000677168.1:n.1164G>T
|
|
|
|
ENST00000677185.1:n.1255G>T
|
|
|
|
ENST00000677205.1:n.1476G>T
|
|
|
|
ENST00000677344.1:n.1966G>T
|
|
|
|
ENST00000677480.1:c.*369G>T
|
ENSP00000504378.1:n.*369G>T
|
|
|
ENST00000677519.1:n.1402G>T
|
|
|
|
ENST00000677593.1:n.1248G>T
|
|
|
|
ENST00000677740.1:n.2197G>T
|
|
|
|
ENST00000677991.1:n.1865G>T
|
|
|
|
ENST00000678001.1:n.1185G>T
|
|
|
|
ENST00000678085.1:n.1248G>T
|
|
|
|
ENST00000678177.1:n.2541G>T
|
|
|
|
ENST00000678603.1:n.1770G>T
|
|
|
|
ENST00000678724.1:c.617G>T
|
ENSP00000503874.1:p.Arg206Leu
|
|
|
ENST00000678920.1:n.850G>T
|
|
|
|
ENST00000679019.1:n.1462G>T
|
|
|
|
ENST00000679117.1:c.*507G>T
|
ENSP00000503240.1:n.*507G>T
|
|
|
ENST00000679339.1:n.1533G>T
|
|
|
|
ENST00000326739.8:c.692G>T
|
ENSP00000321584.4:p.Arg231Leu
|
|
|
ENST00000429182.5:c.486G>T
|
|
|
|
ENST00000442157.1:c.617G>T
|
ENSP00000403502.1:p.Arg206Leu
|
|
|
ENST00000462980.1:n.594G>T
|
|
|
|
ENST00000491610.1:n.652G>T
|
|
|
|
NM_000884.2:c.692G>T
|
NP_000875.2:p.Arg231Leu
|
|
|
XM_006713128.2:c.902G>T
|
XP_006713191.1:p.Arg301Leu
|
|
|
XM_006713128.3:c.902G>T
|
XP_006713191.1:p.Arg301Leu
|
|
|
XM_017006349.1:c.827G>T
|
XP_016861838.1:p.Arg276Leu
|
|
|
XM_017006350.1:c.827G>T
|
XP_016861839.1:p.Arg276Leu
|
|
|
NM_000884.3:c.692G>T
MANE Select
|
NP_000875.2:p.Arg231Leu
|
|
