|
ENST00000703936.1:c.2644C>T
|
ENSP00000515567.1:p.Gln882Ter
|
|
|
ENST00000703937.1:c.*1705C>T
|
ENSP00000515568.1:n.*1705C>T
|
|
|
ENST00000326739.9:c.604C>T
MANE Select
|
ENSP00000321584.4:p.Gln202Ter
|
|
|
ENST00000429182.6:c.604C>T
|
ENSP00000393525.2:p.Gln202Ter
|
|
|
ENST00000442157.2:c.529C>T
|
ENSP00000403502.2:p.Gln177Ter
|
|
|
ENST00000462980.2:n.1119C>T
|
|
|
|
ENST00000472328.2:n.670C>T
|
|
|
|
ENST00000491610.2:n.491C>T
|
|
|
|
ENST00000676607.1:n.900C>T
|
|
|
|
ENST00000676627.1:n.1334C>T
|
|
|
|
ENST00000676708.1:n.1811C>T
|
|
|
|
ENST00000676864.1:n.1680C>T
|
|
|
|
ENST00000677010.1:c.640C>T
|
ENSP00000503089.1:p.Gln214Ter
|
|
|
ENST00000677108.1:n.2437C>T
|
|
|
|
ENST00000677168.1:n.1076C>T
|
|
|
|
ENST00000677185.1:n.1094C>T
|
|
|
|
ENST00000677205.1:n.1315C>T
|
|
|
|
ENST00000677344.1:n.1805C>T
|
|
|
|
ENST00000677480.1:c.*281C>T
|
ENSP00000504378.1:n.*281C>T
|
|
|
ENST00000677519.1:n.1314C>T
|
|
|
|
ENST00000677593.1:n.1087C>T
|
|
|
|
ENST00000677740.1:n.2036C>T
|
|
|
|
ENST00000677991.1:n.1777C>T
|
|
|
|
ENST00000678001.1:n.1097C>T
|
|
|
|
ENST00000678085.1:n.1087C>T
|
|
|
|
ENST00000678177.1:n.2380C>T
|
|
|
|
ENST00000678603.1:n.1682C>T
|
|
|
|
ENST00000678724.1:c.529C>T
|
ENSP00000503874.1:p.Gln177Ter
|
|
|
ENST00000678920.1:n.762C>T
|
|
|
|
ENST00000679019.1:n.1301C>T
|
|
|
|
ENST00000679117.1:c.*419C>T
|
ENSP00000503240.1:n.*419C>T
|
|
|
ENST00000679339.1:n.1372C>T
|
|
|
|
ENST00000326739.8:c.604C>T
|
ENSP00000321584.4:p.Gln202Ter
|
|
|
ENST00000429182.5:c.398C>T
|
|
|
|
ENST00000442157.1:c.529C>T
|
ENSP00000403502.1:p.Gln177Ter
|
|
|
ENST00000462980.1:n.506C>T
|
|
|
|
ENST00000491610.1:n.491C>T
|
|
|
|
NM_000884.2:c.604C>T
|
NP_000875.2:p.Gln202Ter
|
|
|
XM_006713128.2:c.814C>T
|
XP_006713191.1:p.Gln272Ter
|
|
|
XM_006713128.3:c.814C>T
|
XP_006713191.1:p.Gln272Ter
|
|
|
XM_017006349.1:c.739C>T
|
XP_016861838.1:p.Gln247Ter
|
|
|
XM_017006350.1:c.739C>T
|
XP_016861839.1:p.Gln247Ter
|
|
|
NM_000884.3:c.604C>T
MANE Select
|
NP_000875.2:p.Gln202Ter
|
|
