|
ENST00000703936.1:c.2720T>G
|
ENSP00000515567.1:p.Leu907Arg
|
|
|
ENST00000703937.1:c.*1781T>G
|
ENSP00000515568.1:n.*1781T>G
|
|
|
ENST00000326739.9:c.680T>G
MANE Select
|
ENSP00000321584.4:p.Leu227Arg
|
|
|
ENST00000429182.6:c.680T>G
|
ENSP00000393525.2:p.Leu227Arg
|
|
|
ENST00000442157.2:c.605T>G
|
ENSP00000403502.2:p.Leu202Arg
|
|
|
ENST00000462980.2:n.1195T>G
|
|
|
|
ENST00000472328.2:n.746T>G
|
|
|
|
ENST00000491610.2:n.640T>G
|
|
|
|
ENST00000676607.1:n.976T>G
|
|
|
|
ENST00000676627.1:n.1410T>G
|
|
|
|
ENST00000676708.1:n.1960T>G
|
|
|
|
ENST00000676864.1:n.1829T>G
|
|
|
|
ENST00000677010.1:c.716T>G
|
ENSP00000503089.1:p.Leu239Arg
|
|
|
ENST00000677108.1:n.2586T>G
|
|
|
|
ENST00000677168.1:n.1152T>G
|
|
|
|
ENST00000677185.1:n.1243T>G
|
|
|
|
ENST00000677205.1:n.1464T>G
|
|
|
|
ENST00000677344.1:n.1954T>G
|
|
|
|
ENST00000677480.1:c.*357T>G
|
ENSP00000504378.1:n.*357T>G
|
|
|
ENST00000677519.1:n.1390T>G
|
|
|
|
ENST00000677593.1:n.1236T>G
|
|
|
|
ENST00000677740.1:n.2185T>G
|
|
|
|
ENST00000677991.1:n.1853T>G
|
|
|
|
ENST00000678001.1:n.1173T>G
|
|
|
|
ENST00000678085.1:n.1236T>G
|
|
|
|
ENST00000678177.1:n.2529T>G
|
|
|
|
ENST00000678603.1:n.1758T>G
|
|
|
|
ENST00000678724.1:c.605T>G
|
ENSP00000503874.1:p.Leu202Arg
|
|
|
ENST00000678920.1:n.838T>G
|
|
|
|
ENST00000679019.1:n.1450T>G
|
|
|
|
ENST00000679117.1:c.*495T>G
|
ENSP00000503240.1:n.*495T>G
|
|
|
ENST00000679339.1:n.1521T>G
|
|
|
|
ENST00000326739.8:c.680T>G
|
ENSP00000321584.4:p.Leu227Arg
|
|
|
ENST00000429182.5:c.474T>G
|
|
|
|
ENST00000442157.1:c.605T>G
|
ENSP00000403502.1:p.Leu202Arg
|
|
|
ENST00000462980.1:n.582T>G
|
|
|
|
ENST00000491610.1:n.640T>G
|
|
|
|
NM_000884.2:c.680T>G
|
NP_000875.2:p.Leu227Arg
|
|
|
XM_006713128.2:c.890T>G
|
XP_006713191.1:p.Leu297Arg
|
|
|
XM_006713128.3:c.890T>G
|
XP_006713191.1:p.Leu297Arg
|
|
|
XM_017006349.1:c.815T>G
|
XP_016861838.1:p.Leu272Arg
|
|
|
XM_017006350.1:c.815T>G
|
XP_016861839.1:p.Leu272Arg
|
|
|
NM_000884.3:c.680T>G
MANE Select
|
NP_000875.2:p.Leu227Arg
|
|
