|
ENST00000703936.1:c.2677A>C
|
ENSP00000515567.1:p.Asn893His
|
|
|
ENST00000703937.1:c.*1738A>C
|
ENSP00000515568.1:n.*1738A>C
|
|
|
ENST00000326739.9:c.637A>C
MANE Select
|
ENSP00000321584.4:p.Asn213His
|
|
|
ENST00000429182.6:c.637A>C
|
ENSP00000393525.2:p.Asn213His
|
|
|
ENST00000442157.2:c.562A>C
|
ENSP00000403502.2:p.Asn188His
|
|
|
ENST00000462980.2:n.1152A>C
|
|
|
|
ENST00000472328.2:n.703A>C
|
|
|
|
ENST00000491610.2:n.597A>C
|
|
|
|
ENST00000676607.1:n.933A>C
|
|
|
|
ENST00000676627.1:n.1367A>C
|
|
|
|
ENST00000676708.1:n.1917A>C
|
|
|
|
ENST00000676864.1:n.1786A>C
|
|
|
|
ENST00000677010.1:c.673A>C
|
ENSP00000503089.1:p.Asn225His
|
|
|
ENST00000677108.1:n.2543A>C
|
|
|
|
ENST00000677168.1:n.1109A>C
|
|
|
|
ENST00000677185.1:n.1200A>C
|
|
|
|
ENST00000677205.1:n.1421A>C
|
|
|
|
ENST00000677344.1:n.1911A>C
|
|
|
|
ENST00000677480.1:c.*314A>C
|
ENSP00000504378.1:n.*314A>C
|
|
|
ENST00000677519.1:n.1347A>C
|
|
|
|
ENST00000677593.1:n.1193A>C
|
|
|
|
ENST00000677740.1:n.2142A>C
|
|
|
|
ENST00000677991.1:n.1810A>C
|
|
|
|
ENST00000678001.1:n.1130A>C
|
|
|
|
ENST00000678085.1:n.1193A>C
|
|
|
|
ENST00000678177.1:n.2486A>C
|
|
|
|
ENST00000678603.1:n.1715A>C
|
|
|
|
ENST00000678724.1:c.562A>C
|
ENSP00000503874.1:p.Asn188His
|
|
|
ENST00000678920.1:n.795A>C
|
|
|
|
ENST00000679019.1:n.1407A>C
|
|
|
|
ENST00000679117.1:c.*452A>C
|
ENSP00000503240.1:n.*452A>C
|
|
|
ENST00000679339.1:n.1478A>C
|
|
|
|
ENST00000326739.8:c.637A>C
|
ENSP00000321584.4:p.Asn213His
|
|
|
ENST00000429182.5:c.431A>C
|
|
|
|
ENST00000442157.1:c.562A>C
|
ENSP00000403502.1:p.Asn188His
|
|
|
ENST00000462980.1:n.539A>C
|
|
|
|
ENST00000491610.1:n.597A>C
|
|
|
|
NM_000884.2:c.637A>C
|
NP_000875.2:p.Asn213His
|
|
|
XM_006713128.2:c.847A>C
|
XP_006713191.1:p.Asn283His
|
|
|
XM_006713128.3:c.847A>C
|
XP_006713191.1:p.Asn283His
|
|
|
XM_017006349.1:c.772A>C
|
XP_016861838.1:p.Asn258His
|
|
|
XM_017006350.1:c.772A>C
|
XP_016861839.1:p.Asn258His
|
|
|
NM_000884.3:c.637A>C
MANE Select
|
NP_000875.2:p.Asn213His
|
|
