ENST00000703936.1:c.2714C>T
|
ENSP00000515567.1:p.Thr905Ile
|
|
ENST00000703937.1:c.*1775C>T
|
ENSP00000515568.1:n.*1775C>T
|
|
ENST00000326739.9:c.674C>T
MANE Select
|
ENSP00000321584.4:p.Thr225Ile
|
|
ENST00000429182.6:c.674C>T
|
ENSP00000393525.2:p.Thr225Ile
|
|
ENST00000442157.2:c.599C>T
|
ENSP00000403502.2:p.Thr200Ile
|
|
ENST00000462980.2:n.1189C>T
|
|
|
ENST00000472328.2:n.740C>T
|
|
|
ENST00000491610.2:n.634C>T
|
|
|
ENST00000676607.1:n.970C>T
|
|
|
ENST00000676627.1:n.1404C>T
|
|
|
ENST00000676708.1:n.1954C>T
|
|
|
ENST00000676864.1:n.1823C>T
|
|
|
ENST00000677010.1:c.710C>T
|
ENSP00000503089.1:p.Thr237Ile
|
|
ENST00000677108.1:n.2580C>T
|
|
|
ENST00000677168.1:n.1146C>T
|
|
|
ENST00000677185.1:n.1237C>T
|
|
|
ENST00000677205.1:n.1458C>T
|
|
|
ENST00000677344.1:n.1948C>T
|
|
|
ENST00000677480.1:c.*351C>T
|
ENSP00000504378.1:n.*351C>T
|
|
ENST00000677519.1:n.1384C>T
|
|
|
ENST00000677593.1:n.1230C>T
|
|
|
ENST00000677740.1:n.2179C>T
|
|
|
ENST00000677991.1:n.1847C>T
|
|
|
ENST00000678001.1:n.1167C>T
|
|
|
ENST00000678085.1:n.1230C>T
|
|
|
ENST00000678177.1:n.2523C>T
|
|
|
ENST00000678603.1:n.1752C>T
|
|
|
ENST00000678724.1:c.599C>T
|
ENSP00000503874.1:p.Thr200Ile
|
|
ENST00000678920.1:n.832C>T
|
|
|
ENST00000679019.1:n.1444C>T
|
|
|
ENST00000679117.1:c.*489C>T
|
ENSP00000503240.1:n.*489C>T
|
|
ENST00000679339.1:n.1515C>T
|
|
|
ENST00000326739.8:c.674C>T
|
ENSP00000321584.4:p.Thr225Ile
|
|
ENST00000429182.5:c.468C>T
|
|
|
ENST00000442157.1:c.599C>T
|
ENSP00000403502.1:p.Thr200Ile
|
|
ENST00000462980.1:n.576C>T
|
|
|
ENST00000491610.1:n.634C>T
|
|
|
NM_000884.2:c.674C>T
|
NP_000875.2:p.Thr225Ile
|
|
XM_006713128.2:c.884C>T
|
XP_006713191.1:p.Thr295Ile
|
|
XM_006713128.3:c.884C>T
|
XP_006713191.1:p.Thr295Ile
|
|
XM_017006349.1:c.809C>T
|
XP_016861838.1:p.Thr270Ile
|
|
XM_017006350.1:c.809C>T
|
XP_016861839.1:p.Thr270Ile
|
|
NM_000884.3:c.674C>T
MANE Select
|
NP_000875.2:p.Thr225Ile
|
|