|
ENST00000703936.1:c.2861A>C
|
ENSP00000515567.1:p.Asp954Ala
|
|
|
ENST00000703937.1:c.*1922A>C
|
ENSP00000515568.1:n.*1922A>C
|
|
|
ENST00000326739.9:c.821A>C
MANE Select
|
ENSP00000321584.4:p.Asp274Ala
|
|
|
ENST00000429182.6:c.821A>C
|
ENSP00000393525.2:p.Asp274Ala
|
|
|
ENST00000442157.2:c.746A>C
|
ENSP00000403502.2:p.Asp249Ala
|
|
|
ENST00000462980.2:n.1336A>C
|
|
|
|
ENST00000472328.2:n.887A>C
|
|
|
|
ENST00000491610.2:n.781A>C
|
|
|
|
ENST00000676607.1:n.1117A>C
|
|
|
|
ENST00000676627.1:n.1551A>C
|
|
|
|
ENST00000676708.1:n.2101A>C
|
|
|
|
ENST00000676864.1:n.1970A>C
|
|
|
|
ENST00000677010.1:c.856-11A>C
|
ENSP00000503089.1:n.856-11A>C
|
|
|
ENST00000677108.1:n.2804A>C
|
|
|
|
ENST00000677168.1:n.1293A>C
|
|
|
|
ENST00000677185.1:n.1384A>C
|
|
|
|
ENST00000677205.1:n.1605A>C
|
|
|
|
ENST00000677344.1:n.2095A>C
|
|
|
|
ENST00000677480.1:c.*498A>C
|
ENSP00000504378.1:n.*498A>C
|
|
|
ENST00000677519.1:n.1531A>C
|
|
|
|
ENST00000677593.1:n.1377A>C
|
|
|
|
ENST00000677740.1:n.2326A>C
|
|
|
|
ENST00000677991.1:n.1994A>C
|
|
|
|
ENST00000678001.1:n.1314A>C
|
|
|
|
ENST00000678085.1:n.1454A>C
|
|
|
|
ENST00000678177.1:n.2747A>C
|
|
|
|
ENST00000678603.1:n.1899A>C
|
|
|
|
ENST00000678724.1:c.746A>C
|
ENSP00000503874.1:p.Asp249Ala
|
|
|
ENST00000678920.1:n.979A>C
|
|
|
|
ENST00000679019.1:n.1668A>C
|
|
|
|
ENST00000679117.1:c.*636A>C
|
ENSP00000503240.1:n.*636A>C
|
|
|
ENST00000679339.1:n.1662A>C
|
|
|
|
ENST00000326739.8:c.821A>C
|
ENSP00000321584.4:p.Asp274Ala
|
|
|
ENST00000429182.5:c.615A>C
|
|
|
|
ENST00000442157.1:c.746A>C
|
ENSP00000403502.1:p.Asp249Ala
|
|
|
ENST00000462980.1:n.723A>C
|
|
|
|
ENST00000491610.1:n.781A>C
|
|
|
|
NM_000884.2:c.821A>C
|
NP_000875.2:p.Asp274Ala
|
|
|
XM_006713128.2:c.1031A>C
|
XP_006713191.1:p.Asp344Ala
|
|
|
XM_006713128.3:c.1031A>C
|
XP_006713191.1:p.Asp344Ala
|
|
|
XM_017006349.1:c.956A>C
|
XP_016861838.1:p.Asp319Ala
|
|
|
XM_017006350.1:c.956A>C
|
XP_016861839.1:p.Asp319Ala
|
|
|
NM_000884.3:c.821A>C
MANE Select
|
NP_000875.2:p.Asp274Ala
|
|
