|
ENST00000703936.1:c.2734G>C
|
ENSP00000515567.1:p.Asp912His
|
|
|
ENST00000703937.1:c.*1795G>C
|
ENSP00000515568.1:n.*1795G>C
|
|
|
ENST00000326739.9:c.694G>C
MANE Select
|
ENSP00000321584.4:p.Asp232His
|
|
|
ENST00000429182.6:c.694G>C
|
ENSP00000393525.2:p.Asp232His
|
|
|
ENST00000442157.2:c.619G>C
|
ENSP00000403502.2:p.Asp207His
|
|
|
ENST00000462980.2:n.1209G>C
|
|
|
|
ENST00000472328.2:n.760G>C
|
|
|
|
ENST00000491610.2:n.654G>C
|
|
|
|
ENST00000676607.1:n.990G>C
|
|
|
|
ENST00000676627.1:n.1424G>C
|
|
|
|
ENST00000676708.1:n.1974G>C
|
|
|
|
ENST00000676864.1:n.1843G>C
|
|
|
|
ENST00000677010.1:c.730G>C
|
ENSP00000503089.1:p.Asp244His
|
|
|
ENST00000677108.1:n.2600G>C
|
|
|
|
ENST00000677168.1:n.1166G>C
|
|
|
|
ENST00000677185.1:n.1257G>C
|
|
|
|
ENST00000677205.1:n.1478G>C
|
|
|
|
ENST00000677344.1:n.1968G>C
|
|
|
|
ENST00000677480.1:c.*371G>C
|
ENSP00000504378.1:n.*371G>C
|
|
|
ENST00000677519.1:n.1404G>C
|
|
|
|
ENST00000677593.1:n.1250G>C
|
|
|
|
ENST00000677740.1:n.2199G>C
|
|
|
|
ENST00000677991.1:n.1867G>C
|
|
|
|
ENST00000678001.1:n.1187G>C
|
|
|
|
ENST00000678085.1:n.1250G>C
|
|
|
|
ENST00000678177.1:n.2543G>C
|
|
|
|
ENST00000678603.1:n.1772G>C
|
|
|
|
ENST00000678724.1:c.619G>C
|
ENSP00000503874.1:p.Asp207His
|
|
|
ENST00000678920.1:n.852G>C
|
|
|
|
ENST00000679019.1:n.1464G>C
|
|
|
|
ENST00000679117.1:c.*509G>C
|
ENSP00000503240.1:n.*509G>C
|
|
|
ENST00000679339.1:n.1535G>C
|
|
|
|
ENST00000326739.8:c.694G>C
|
ENSP00000321584.4:p.Asp232His
|
|
|
ENST00000429182.5:c.488G>C
|
|
|
|
ENST00000442157.1:c.619G>C
|
ENSP00000403502.1:p.Asp207His
|
|
|
ENST00000462980.1:n.596G>C
|
|
|
|
ENST00000491610.1:n.654G>C
|
|
|
|
NM_000884.2:c.694G>C
|
NP_000875.2:p.Asp232His
|
|
|
XM_006713128.2:c.904G>C
|
XP_006713191.1:p.Asp302His
|
|
|
XM_006713128.3:c.904G>C
|
XP_006713191.1:p.Asp302His
|
|
|
XM_017006349.1:c.829G>C
|
XP_016861838.1:p.Asp277His
|
|
|
XM_017006350.1:c.829G>C
|
XP_016861839.1:p.Asp277His
|
|
|
NM_000884.3:c.694G>C
MANE Select
|
NP_000875.2:p.Asp232His
|
|
