|
ENST00000703936.1:c.2735A>C
|
ENSP00000515567.1:p.Asp912Ala
|
|
|
ENST00000703937.1:c.*1796A>C
|
ENSP00000515568.1:n.*1796A>C
|
|
|
ENST00000326739.9:c.695A>C
MANE Select
|
ENSP00000321584.4:p.Asp232Ala
|
|
|
ENST00000429182.6:c.695A>C
|
ENSP00000393525.2:p.Asp232Ala
|
|
|
ENST00000442157.2:c.620A>C
|
ENSP00000403502.2:p.Asp207Ala
|
|
|
ENST00000462980.2:n.1210A>C
|
|
|
|
ENST00000472328.2:n.761A>C
|
|
|
|
ENST00000491610.2:n.655A>C
|
|
|
|
ENST00000676607.1:n.991A>C
|
|
|
|
ENST00000676627.1:n.1425A>C
|
|
|
|
ENST00000676708.1:n.1975A>C
|
|
|
|
ENST00000676864.1:n.1844A>C
|
|
|
|
ENST00000677010.1:c.731A>C
|
ENSP00000503089.1:p.Asp244Ala
|
|
|
ENST00000677108.1:n.2601A>C
|
|
|
|
ENST00000677168.1:n.1167A>C
|
|
|
|
ENST00000677185.1:n.1258A>C
|
|
|
|
ENST00000677205.1:n.1479A>C
|
|
|
|
ENST00000677344.1:n.1969A>C
|
|
|
|
ENST00000677480.1:c.*372A>C
|
ENSP00000504378.1:n.*372A>C
|
|
|
ENST00000677519.1:n.1405A>C
|
|
|
|
ENST00000677593.1:n.1251A>C
|
|
|
|
ENST00000677740.1:n.2200A>C
|
|
|
|
ENST00000677991.1:n.1868A>C
|
|
|
|
ENST00000678001.1:n.1188A>C
|
|
|
|
ENST00000678085.1:n.1251A>C
|
|
|
|
ENST00000678177.1:n.2544A>C
|
|
|
|
ENST00000678603.1:n.1773A>C
|
|
|
|
ENST00000678724.1:c.620A>C
|
ENSP00000503874.1:p.Asp207Ala
|
|
|
ENST00000678920.1:n.853A>C
|
|
|
|
ENST00000679019.1:n.1465A>C
|
|
|
|
ENST00000679117.1:c.*510A>C
|
ENSP00000503240.1:n.*510A>C
|
|
|
ENST00000679339.1:n.1536A>C
|
|
|
|
ENST00000326739.8:c.695A>C
|
ENSP00000321584.4:p.Asp232Ala
|
|
|
ENST00000429182.5:c.489A>C
|
|
|
|
ENST00000442157.1:c.620A>C
|
ENSP00000403502.1:p.Asp207Ala
|
|
|
ENST00000462980.1:n.597A>C
|
|
|
|
ENST00000491610.1:n.655A>C
|
|
|
|
NM_000884.2:c.695A>C
|
NP_000875.2:p.Asp232Ala
|
|
|
XM_006713128.2:c.905A>C
|
XP_006713191.1:p.Asp302Ala
|
|
|
XM_006713128.3:c.905A>C
|
XP_006713191.1:p.Asp302Ala
|
|
|
XM_017006349.1:c.830A>C
|
XP_016861838.1:p.Asp277Ala
|
|
|
XM_017006350.1:c.830A>C
|
XP_016861839.1:p.Asp277Ala
|
|
|
NM_000884.3:c.695A>C
MANE Select
|
NP_000875.2:p.Asp232Ala
|
|
