|
ENST00000703936.1:c.2642T>A
|
ENSP00000515567.1:p.Leu881Gln
|
|
|
ENST00000703937.1:c.*1703T>A
|
ENSP00000515568.1:n.*1703T>A
|
|
|
ENST00000326739.9:c.602T>A
MANE Select
|
ENSP00000321584.4:p.Leu201Gln
|
|
|
ENST00000429182.6:c.602T>A
|
ENSP00000393525.2:p.Leu201Gln
|
|
|
ENST00000442157.2:c.527T>A
|
ENSP00000403502.2:p.Leu176Gln
|
|
|
ENST00000462980.2:n.1117T>A
|
|
|
|
ENST00000472328.2:n.668T>A
|
|
|
|
ENST00000491610.2:n.489T>A
|
|
|
|
ENST00000676607.1:n.898T>A
|
|
|
|
ENST00000676627.1:n.1332T>A
|
|
|
|
ENST00000676708.1:n.1809T>A
|
|
|
|
ENST00000676864.1:n.1678T>A
|
|
|
|
ENST00000677010.1:c.638T>A
|
ENSP00000503089.1:p.Leu213Gln
|
|
|
ENST00000677108.1:n.2435T>A
|
|
|
|
ENST00000677168.1:n.1074T>A
|
|
|
|
ENST00000677185.1:n.1092T>A
|
|
|
|
ENST00000677205.1:n.1313T>A
|
|
|
|
ENST00000677344.1:n.1803T>A
|
|
|
|
ENST00000677480.1:c.*279T>A
|
ENSP00000504378.1:n.*279T>A
|
|
|
ENST00000677519.1:n.1312T>A
|
|
|
|
ENST00000677593.1:n.1085T>A
|
|
|
|
ENST00000677740.1:n.2034T>A
|
|
|
|
ENST00000677991.1:n.1775T>A
|
|
|
|
ENST00000678001.1:n.1095T>A
|
|
|
|
ENST00000678085.1:n.1085T>A
|
|
|
|
ENST00000678177.1:n.2378T>A
|
|
|
|
ENST00000678603.1:n.1680T>A
|
|
|
|
ENST00000678724.1:c.527T>A
|
ENSP00000503874.1:p.Leu176Gln
|
|
|
ENST00000678920.1:n.760T>A
|
|
|
|
ENST00000679019.1:n.1299T>A
|
|
|
|
ENST00000679117.1:c.*417T>A
|
ENSP00000503240.1:n.*417T>A
|
|
|
ENST00000679339.1:n.1370T>A
|
|
|
|
ENST00000326739.8:c.602T>A
|
ENSP00000321584.4:p.Leu201Gln
|
|
|
ENST00000429182.5:c.396T>A
|
|
|
|
ENST00000442157.1:c.527T>A
|
ENSP00000403502.1:p.Leu176Gln
|
|
|
ENST00000462980.1:n.504T>A
|
|
|
|
ENST00000491610.1:n.489T>A
|
|
|
|
NM_000884.2:c.602T>A
|
NP_000875.2:p.Leu201Gln
|
|
|
XM_006713128.2:c.812T>A
|
XP_006713191.1:p.Leu271Gln
|
|
|
XM_006713128.3:c.812T>A
|
XP_006713191.1:p.Leu271Gln
|
|
|
XM_017006349.1:c.737T>A
|
XP_016861838.1:p.Leu246Gln
|
|
|
XM_017006350.1:c.737T>A
|
XP_016861839.1:p.Leu246Gln
|
|
|
NM_000884.3:c.602T>A
MANE Select
|
NP_000875.2:p.Leu201Gln
|
|
