|
ENST00000703936.1:c.2708C>G
|
ENSP00000515567.1:p.Ala903Gly
|
|
|
ENST00000703937.1:c.*1769C>G
|
ENSP00000515568.1:n.*1769C>G
|
|
|
ENST00000326739.9:c.668C>G
MANE Select
|
ENSP00000321584.4:p.Ala223Gly
|
|
|
ENST00000429182.6:c.668C>G
|
ENSP00000393525.2:p.Ala223Gly
|
|
|
ENST00000442157.2:c.593C>G
|
ENSP00000403502.2:p.Ala198Gly
|
|
|
ENST00000462980.2:n.1183C>G
|
|
|
|
ENST00000472328.2:n.734C>G
|
|
|
|
ENST00000491610.2:n.628C>G
|
|
|
|
ENST00000676607.1:n.964C>G
|
|
|
|
ENST00000676627.1:n.1398C>G
|
|
|
|
ENST00000676708.1:n.1948C>G
|
|
|
|
ENST00000676864.1:n.1817C>G
|
|
|
|
ENST00000677010.1:c.704C>G
|
ENSP00000503089.1:p.Ala235Gly
|
|
|
ENST00000677108.1:n.2574C>G
|
|
|
|
ENST00000677168.1:n.1140C>G
|
|
|
|
ENST00000677185.1:n.1231C>G
|
|
|
|
ENST00000677205.1:n.1452C>G
|
|
|
|
ENST00000677344.1:n.1942C>G
|
|
|
|
ENST00000677480.1:c.*345C>G
|
ENSP00000504378.1:n.*345C>G
|
|
|
ENST00000677519.1:n.1378C>G
|
|
|
|
ENST00000677593.1:n.1224C>G
|
|
|
|
ENST00000677740.1:n.2173C>G
|
|
|
|
ENST00000677991.1:n.1841C>G
|
|
|
|
ENST00000678001.1:n.1161C>G
|
|
|
|
ENST00000678085.1:n.1224C>G
|
|
|
|
ENST00000678177.1:n.2517C>G
|
|
|
|
ENST00000678603.1:n.1746C>G
|
|
|
|
ENST00000678724.1:c.593C>G
|
ENSP00000503874.1:p.Ala198Gly
|
|
|
ENST00000678920.1:n.826C>G
|
|
|
|
ENST00000679019.1:n.1438C>G
|
|
|
|
ENST00000679117.1:c.*483C>G
|
ENSP00000503240.1:n.*483C>G
|
|
|
ENST00000679339.1:n.1509C>G
|
|
|
|
ENST00000326739.8:c.668C>G
|
ENSP00000321584.4:p.Ala223Gly
|
|
|
ENST00000429182.5:c.462C>G
|
|
|
|
ENST00000442157.1:c.593C>G
|
ENSP00000403502.1:p.Ala198Gly
|
|
|
ENST00000462980.1:n.570C>G
|
|
|
|
ENST00000491610.1:n.628C>G
|
|
|
|
NM_000884.2:c.668C>G
|
NP_000875.2:p.Ala223Gly
|
|
|
XM_006713128.2:c.878C>G
|
XP_006713191.1:p.Ala293Gly
|
|
|
XM_006713128.3:c.878C>G
|
XP_006713191.1:p.Ala293Gly
|
|
|
XM_017006349.1:c.803C>G
|
XP_016861838.1:p.Ala268Gly
|
|
|
XM_017006350.1:c.803C>G
|
XP_016861839.1:p.Ala268Gly
|
|
|
NM_000884.3:c.668C>G
MANE Select
|
NP_000875.2:p.Ala223Gly
|
|
