|
ENST00000703936.1:c.2860G>C
|
ENSP00000515567.1:p.Asp954His
|
|
|
ENST00000703937.1:c.*1921G>C
|
ENSP00000515568.1:n.*1921G>C
|
|
|
ENST00000326739.9:c.820G>C
MANE Select
|
ENSP00000321584.4:p.Asp274His
|
|
|
ENST00000429182.6:c.820G>C
|
ENSP00000393525.2:p.Asp274His
|
|
|
ENST00000442157.2:c.745G>C
|
ENSP00000403502.2:p.Asp249His
|
|
|
ENST00000462980.2:n.1335G>C
|
|
|
|
ENST00000472328.2:n.886G>C
|
|
|
|
ENST00000491610.2:n.780G>C
|
|
|
|
ENST00000676607.1:n.1116G>C
|
|
|
|
ENST00000676627.1:n.1550G>C
|
|
|
|
ENST00000676708.1:n.2100G>C
|
|
|
|
ENST00000676864.1:n.1969G>C
|
|
|
|
ENST00000677010.1:c.856-12G>C
|
ENSP00000503089.1:n.856-12G>C
|
|
|
ENST00000677108.1:n.2803G>C
|
|
|
|
ENST00000677168.1:n.1292G>C
|
|
|
|
ENST00000677185.1:n.1383G>C
|
|
|
|
ENST00000677205.1:n.1604G>C
|
|
|
|
ENST00000677344.1:n.2094G>C
|
|
|
|
ENST00000677480.1:c.*497G>C
|
ENSP00000504378.1:n.*497G>C
|
|
|
ENST00000677519.1:n.1530G>C
|
|
|
|
ENST00000677593.1:n.1376G>C
|
|
|
|
ENST00000677740.1:n.2325G>C
|
|
|
|
ENST00000677991.1:n.1993G>C
|
|
|
|
ENST00000678001.1:n.1313G>C
|
|
|
|
ENST00000678085.1:n.1453G>C
|
|
|
|
ENST00000678177.1:n.2746G>C
|
|
|
|
ENST00000678603.1:n.1898G>C
|
|
|
|
ENST00000678724.1:c.745G>C
|
ENSP00000503874.1:p.Asp249His
|
|
|
ENST00000678920.1:n.978G>C
|
|
|
|
ENST00000679019.1:n.1667G>C
|
|
|
|
ENST00000679117.1:c.*635G>C
|
ENSP00000503240.1:n.*635G>C
|
|
|
ENST00000679339.1:n.1661G>C
|
|
|
|
ENST00000326739.8:c.820G>C
|
ENSP00000321584.4:p.Asp274His
|
|
|
ENST00000429182.5:c.614G>C
|
|
|
|
ENST00000442157.1:c.745G>C
|
ENSP00000403502.1:p.Asp249His
|
|
|
ENST00000462980.1:n.722G>C
|
|
|
|
ENST00000491610.1:n.780G>C
|
|
|
|
NM_000884.2:c.820G>C
|
NP_000875.2:p.Asp274His
|
|
|
XM_006713128.2:c.1030G>C
|
XP_006713191.1:p.Asp344His
|
|
|
XM_006713128.3:c.1030G>C
|
XP_006713191.1:p.Asp344His
|
|
|
XM_017006349.1:c.955G>C
|
XP_016861838.1:p.Asp319His
|
|
|
XM_017006350.1:c.955G>C
|
XP_016861839.1:p.Asp319His
|
|
|
NM_000884.3:c.820G>C
MANE Select
|
NP_000875.2:p.Asp274His
|
|
