|
ENST00000703936.1:c.2686G>C
|
ENSP00000515567.1:p.Asp896His
|
|
|
ENST00000703937.1:c.*1747G>C
|
ENSP00000515568.1:n.*1747G>C
|
|
|
ENST00000326739.9:c.646G>C
MANE Select
|
ENSP00000321584.4:p.Asp216His
|
|
|
ENST00000429182.6:c.646G>C
|
ENSP00000393525.2:p.Asp216His
|
|
|
ENST00000442157.2:c.571G>C
|
ENSP00000403502.2:p.Asp191His
|
|
|
ENST00000462980.2:n.1161G>C
|
|
|
|
ENST00000472328.2:n.712G>C
|
|
|
|
ENST00000491610.2:n.606G>C
|
|
|
|
ENST00000676607.1:n.942G>C
|
|
|
|
ENST00000676627.1:n.1376G>C
|
|
|
|
ENST00000676708.1:n.1926G>C
|
|
|
|
ENST00000676864.1:n.1795G>C
|
|
|
|
ENST00000677010.1:c.682G>C
|
ENSP00000503089.1:p.Asp228His
|
|
|
ENST00000677108.1:n.2552G>C
|
|
|
|
ENST00000677168.1:n.1118G>C
|
|
|
|
ENST00000677185.1:n.1209G>C
|
|
|
|
ENST00000677205.1:n.1430G>C
|
|
|
|
ENST00000677344.1:n.1920G>C
|
|
|
|
ENST00000677480.1:c.*323G>C
|
ENSP00000504378.1:n.*323G>C
|
|
|
ENST00000677519.1:n.1356G>C
|
|
|
|
ENST00000677593.1:n.1202G>C
|
|
|
|
ENST00000677740.1:n.2151G>C
|
|
|
|
ENST00000677991.1:n.1819G>C
|
|
|
|
ENST00000678001.1:n.1139G>C
|
|
|
|
ENST00000678085.1:n.1202G>C
|
|
|
|
ENST00000678177.1:n.2495G>C
|
|
|
|
ENST00000678603.1:n.1724G>C
|
|
|
|
ENST00000678724.1:c.571G>C
|
ENSP00000503874.1:p.Asp191His
|
|
|
ENST00000678920.1:n.804G>C
|
|
|
|
ENST00000679019.1:n.1416G>C
|
|
|
|
ENST00000679117.1:c.*461G>C
|
ENSP00000503240.1:n.*461G>C
|
|
|
ENST00000679339.1:n.1487G>C
|
|
|
|
ENST00000326739.8:c.646G>C
|
ENSP00000321584.4:p.Asp216His
|
|
|
ENST00000429182.5:c.440G>C
|
|
|
|
ENST00000442157.1:c.571G>C
|
ENSP00000403502.1:p.Asp191His
|
|
|
ENST00000462980.1:n.548G>C
|
|
|
|
ENST00000491610.1:n.606G>C
|
|
|
|
NM_000884.2:c.646G>C
|
NP_000875.2:p.Asp216His
|
|
|
XM_006713128.2:c.856G>C
|
XP_006713191.1:p.Asp286His
|
|
|
XM_006713128.3:c.856G>C
|
XP_006713191.1:p.Asp286His
|
|
|
XM_017006349.1:c.781G>C
|
XP_016861838.1:p.Asp261His
|
|
|
XM_017006350.1:c.781G>C
|
XP_016861839.1:p.Asp261His
|
|
|
NM_000884.3:c.646G>C
MANE Select
|
NP_000875.2:p.Asp216His
|
|
