|
ENST00000703936.1:c.2673T>G
|
ENSP00000515567.1:p.Ile891Met
|
|
|
ENST00000703937.1:c.*1734T>G
|
ENSP00000515568.1:n.*1734T>G
|
|
|
ENST00000326739.9:c.633T>G
MANE Select
|
ENSP00000321584.4:p.Ile211Met
|
|
|
ENST00000429182.6:c.633T>G
|
ENSP00000393525.2:p.Ile211Met
|
|
|
ENST00000442157.2:c.558T>G
|
ENSP00000403502.2:p.Ile186Met
|
|
|
ENST00000462980.2:n.1148T>G
|
|
|
|
ENST00000472328.2:n.699T>G
|
|
|
|
ENST00000491610.2:n.593T>G
|
|
|
|
ENST00000676607.1:n.929T>G
|
|
|
|
ENST00000676627.1:n.1363T>G
|
|
|
|
ENST00000676708.1:n.1913T>G
|
|
|
|
ENST00000676864.1:n.1782T>G
|
|
|
|
ENST00000677010.1:c.669T>G
|
ENSP00000503089.1:p.Ile223Met
|
|
|
ENST00000677108.1:n.2539T>G
|
|
|
|
ENST00000677168.1:n.1105T>G
|
|
|
|
ENST00000677185.1:n.1196T>G
|
|
|
|
ENST00000677205.1:n.1417T>G
|
|
|
|
ENST00000677344.1:n.1907T>G
|
|
|
|
ENST00000677480.1:c.*310T>G
|
ENSP00000504378.1:n.*310T>G
|
|
|
ENST00000677519.1:n.1343T>G
|
|
|
|
ENST00000677593.1:n.1189T>G
|
|
|
|
ENST00000677740.1:n.2138T>G
|
|
|
|
ENST00000677991.1:n.1806T>G
|
|
|
|
ENST00000678001.1:n.1126T>G
|
|
|
|
ENST00000678085.1:n.1189T>G
|
|
|
|
ENST00000678177.1:n.2482T>G
|
|
|
|
ENST00000678603.1:n.1711T>G
|
|
|
|
ENST00000678724.1:c.558T>G
|
ENSP00000503874.1:p.Ile186Met
|
|
|
ENST00000678920.1:n.791T>G
|
|
|
|
ENST00000679019.1:n.1403T>G
|
|
|
|
ENST00000679117.1:c.*448T>G
|
ENSP00000503240.1:n.*448T>G
|
|
|
ENST00000679339.1:n.1474T>G
|
|
|
|
ENST00000326739.8:c.633T>G
|
ENSP00000321584.4:p.Ile211Met
|
|
|
ENST00000429182.5:c.427T>G
|
|
|
|
ENST00000442157.1:c.558T>G
|
ENSP00000403502.1:p.Ile186Met
|
|
|
ENST00000462980.1:n.535T>G
|
|
|
|
ENST00000491610.1:n.593T>G
|
|
|
|
NM_000884.2:c.633T>G
|
NP_000875.2:p.Ile211Met
|
|
|
XM_006713128.2:c.843T>G
|
XP_006713191.1:p.Ile281Met
|
|
|
XM_006713128.3:c.843T>G
|
XP_006713191.1:p.Ile281Met
|
|
|
XM_017006349.1:c.768T>G
|
XP_016861838.1:p.Ile256Met
|
|
|
XM_017006350.1:c.768T>G
|
XP_016861839.1:p.Ile256Met
|
|
|
NM_000884.3:c.633T>G
MANE Select
|
NP_000875.2:p.Ile211Met
|
|
