|
ENST00000703936.1:c.2710C>G
|
ENSP00000515567.1:p.Arg904Gly
|
|
|
ENST00000703937.1:c.*1771C>G
|
ENSP00000515568.1:n.*1771C>G
|
|
|
ENST00000326739.9:c.670C>G
MANE Select
|
ENSP00000321584.4:p.Arg224Gly
|
|
|
ENST00000429182.6:c.670C>G
|
ENSP00000393525.2:p.Arg224Gly
|
|
|
ENST00000442157.2:c.595C>G
|
ENSP00000403502.2:p.Arg199Gly
|
|
|
ENST00000462980.2:n.1185C>G
|
|
|
|
ENST00000472328.2:n.736C>G
|
|
|
|
ENST00000491610.2:n.630C>G
|
|
|
|
ENST00000676607.1:n.966C>G
|
|
|
|
ENST00000676627.1:n.1400C>G
|
|
|
|
ENST00000676708.1:n.1950C>G
|
|
|
|
ENST00000676864.1:n.1819C>G
|
|
|
|
ENST00000677010.1:c.706C>G
|
ENSP00000503089.1:p.Arg236Gly
|
|
|
ENST00000677108.1:n.2576C>G
|
|
|
|
ENST00000677168.1:n.1142C>G
|
|
|
|
ENST00000677185.1:n.1233C>G
|
|
|
|
ENST00000677205.1:n.1454C>G
|
|
|
|
ENST00000677344.1:n.1944C>G
|
|
|
|
ENST00000677480.1:c.*347C>G
|
ENSP00000504378.1:n.*347C>G
|
|
|
ENST00000677519.1:n.1380C>G
|
|
|
|
ENST00000677593.1:n.1226C>G
|
|
|
|
ENST00000677740.1:n.2175C>G
|
|
|
|
ENST00000677991.1:n.1843C>G
|
|
|
|
ENST00000678001.1:n.1163C>G
|
|
|
|
ENST00000678085.1:n.1226C>G
|
|
|
|
ENST00000678177.1:n.2519C>G
|
|
|
|
ENST00000678603.1:n.1748C>G
|
|
|
|
ENST00000678724.1:c.595C>G
|
ENSP00000503874.1:p.Arg199Gly
|
|
|
ENST00000678920.1:n.828C>G
|
|
|
|
ENST00000679019.1:n.1440C>G
|
|
|
|
ENST00000679117.1:c.*485C>G
|
ENSP00000503240.1:n.*485C>G
|
|
|
ENST00000679339.1:n.1511C>G
|
|
|
|
ENST00000326739.8:c.670C>G
|
ENSP00000321584.4:p.Arg224Gly
|
|
|
ENST00000429182.5:c.464C>G
|
|
|
|
ENST00000442157.1:c.595C>G
|
ENSP00000403502.1:p.Arg199Gly
|
|
|
ENST00000462980.1:n.572C>G
|
|
|
|
ENST00000491610.1:n.630C>G
|
|
|
|
NM_000884.2:c.670C>G
|
NP_000875.2:p.Arg224Gly
|
|
|
XM_006713128.2:c.880C>G
|
XP_006713191.1:p.Arg294Gly
|
|
|
XM_006713128.3:c.880C>G
|
XP_006713191.1:p.Arg294Gly
|
|
|
XM_017006349.1:c.805C>G
|
XP_016861838.1:p.Arg269Gly
|
|
|
XM_017006350.1:c.805C>G
|
XP_016861839.1:p.Arg269Gly
|
|
|
NM_000884.3:c.670C>G
MANE Select
|
NP_000875.2:p.Arg224Gly
|
|
