|
ENST00000703936.1:c.2639T>C
|
ENSP00000515567.1:p.Ile880Thr
|
|
|
ENST00000703937.1:c.*1700T>C
|
ENSP00000515568.1:n.*1700T>C
|
|
|
ENST00000326739.9:c.599T>C
MANE Select
|
ENSP00000321584.4:p.Ile200Thr
|
|
|
ENST00000429182.6:c.599T>C
|
ENSP00000393525.2:p.Ile200Thr
|
|
|
ENST00000442157.2:c.524T>C
|
ENSP00000403502.2:p.Ile175Thr
|
|
|
ENST00000462980.2:n.1114T>C
|
|
|
|
ENST00000472328.2:n.665T>C
|
|
|
|
ENST00000491610.2:n.486T>C
|
|
|
|
ENST00000676607.1:n.895T>C
|
|
|
|
ENST00000676627.1:n.1329T>C
|
|
|
|
ENST00000676708.1:n.1806T>C
|
|
|
|
ENST00000676864.1:n.1675T>C
|
|
|
|
ENST00000677010.1:c.635T>C
|
ENSP00000503089.1:p.Ile212Thr
|
|
|
ENST00000677108.1:n.2432T>C
|
|
|
|
ENST00000677168.1:n.1071T>C
|
|
|
|
ENST00000677185.1:n.1089T>C
|
|
|
|
ENST00000677205.1:n.1310T>C
|
|
|
|
ENST00000677344.1:n.1800T>C
|
|
|
|
ENST00000677480.1:c.*276T>C
|
ENSP00000504378.1:n.*276T>C
|
|
|
ENST00000677519.1:n.1309T>C
|
|
|
|
ENST00000677593.1:n.1082T>C
|
|
|
|
ENST00000677740.1:n.2031T>C
|
|
|
|
ENST00000677991.1:n.1772T>C
|
|
|
|
ENST00000678001.1:n.1092T>C
|
|
|
|
ENST00000678085.1:n.1082T>C
|
|
|
|
ENST00000678177.1:n.2375T>C
|
|
|
|
ENST00000678603.1:n.1677T>C
|
|
|
|
ENST00000678724.1:c.524T>C
|
ENSP00000503874.1:p.Ile175Thr
|
|
|
ENST00000678920.1:n.757T>C
|
|
|
|
ENST00000679019.1:n.1296T>C
|
|
|
|
ENST00000679117.1:c.*414T>C
|
ENSP00000503240.1:n.*414T>C
|
|
|
ENST00000679339.1:n.1367T>C
|
|
|
|
ENST00000326739.8:c.599T>C
|
ENSP00000321584.4:p.Ile200Thr
|
|
|
ENST00000429182.5:c.393T>C
|
|
|
|
ENST00000442157.1:c.524T>C
|
ENSP00000403502.1:p.Ile175Thr
|
|
|
ENST00000462980.1:n.501T>C
|
|
|
|
ENST00000491610.1:n.486T>C
|
|
|
|
NM_000884.2:c.599T>C
|
NP_000875.2:p.Ile200Thr
|
|
|
XM_006713128.2:c.809T>C
|
XP_006713191.1:p.Ile270Thr
|
|
|
XM_006713128.3:c.809T>C
|
XP_006713191.1:p.Ile270Thr
|
|
|
XM_017006349.1:c.734T>C
|
XP_016861838.1:p.Ile245Thr
|
|
|
XM_017006350.1:c.734T>C
|
XP_016861839.1:p.Ile245Thr
|
|
|
NM_000884.3:c.599T>C
MANE Select
|
NP_000875.2:p.Ile200Thr
|
|
