|
ENST00000703936.1:c.2678A>C
|
ENSP00000515567.1:p.Asn893Thr
|
|
|
ENST00000703937.1:c.*1739A>C
|
ENSP00000515568.1:n.*1739A>C
|
|
|
ENST00000326739.9:c.638A>C
MANE Select
|
ENSP00000321584.4:p.Asn213Thr
|
|
|
ENST00000429182.6:c.638A>C
|
ENSP00000393525.2:p.Asn213Thr
|
|
|
ENST00000442157.2:c.563A>C
|
ENSP00000403502.2:p.Asn188Thr
|
|
|
ENST00000462980.2:n.1153A>C
|
|
|
|
ENST00000472328.2:n.704A>C
|
|
|
|
ENST00000491610.2:n.598A>C
|
|
|
|
ENST00000676607.1:n.934A>C
|
|
|
|
ENST00000676627.1:n.1368A>C
|
|
|
|
ENST00000676708.1:n.1918A>C
|
|
|
|
ENST00000676864.1:n.1787A>C
|
|
|
|
ENST00000677010.1:c.674A>C
|
ENSP00000503089.1:p.Asn225Thr
|
|
|
ENST00000677108.1:n.2544A>C
|
|
|
|
ENST00000677168.1:n.1110A>C
|
|
|
|
ENST00000677185.1:n.1201A>C
|
|
|
|
ENST00000677205.1:n.1422A>C
|
|
|
|
ENST00000677344.1:n.1912A>C
|
|
|
|
ENST00000677480.1:c.*315A>C
|
ENSP00000504378.1:n.*315A>C
|
|
|
ENST00000677519.1:n.1348A>C
|
|
|
|
ENST00000677593.1:n.1194A>C
|
|
|
|
ENST00000677740.1:n.2143A>C
|
|
|
|
ENST00000677991.1:n.1811A>C
|
|
|
|
ENST00000678001.1:n.1131A>C
|
|
|
|
ENST00000678085.1:n.1194A>C
|
|
|
|
ENST00000678177.1:n.2487A>C
|
|
|
|
ENST00000678603.1:n.1716A>C
|
|
|
|
ENST00000678724.1:c.563A>C
|
ENSP00000503874.1:p.Asn188Thr
|
|
|
ENST00000678920.1:n.796A>C
|
|
|
|
ENST00000679019.1:n.1408A>C
|
|
|
|
ENST00000679117.1:c.*453A>C
|
ENSP00000503240.1:n.*453A>C
|
|
|
ENST00000679339.1:n.1479A>C
|
|
|
|
ENST00000326739.8:c.638A>C
|
ENSP00000321584.4:p.Asn213Thr
|
|
|
ENST00000429182.5:c.432A>C
|
|
|
|
ENST00000442157.1:c.563A>C
|
ENSP00000403502.1:p.Asn188Thr
|
|
|
ENST00000462980.1:n.540A>C
|
|
|
|
ENST00000491610.1:n.598A>C
|
|
|
|
NM_000884.2:c.638A>C
|
NP_000875.2:p.Asn213Thr
|
|
|
XM_006713128.2:c.848A>C
|
XP_006713191.1:p.Asn283Thr
|
|
|
XM_006713128.3:c.848A>C
|
XP_006713191.1:p.Asn283Thr
|
|
|
XM_017006349.1:c.773A>C
|
XP_016861838.1:p.Asn258Thr
|
|
|
XM_017006350.1:c.773A>C
|
XP_016861839.1:p.Asn258Thr
|
|
|
NM_000884.3:c.638A>C
MANE Select
|
NP_000875.2:p.Asn213Thr
|
|
