|
ENST00000703936.1:c.2702T>G
|
ENSP00000515567.1:p.Ile901Ser
|
|
|
ENST00000703937.1:c.*1763T>G
|
ENSP00000515568.1:n.*1763T>G
|
|
|
ENST00000326739.9:c.662T>G
MANE Select
|
ENSP00000321584.4:p.Ile221Ser
|
|
|
ENST00000429182.6:c.662T>G
|
ENSP00000393525.2:p.Ile221Ser
|
|
|
ENST00000442157.2:c.587T>G
|
ENSP00000403502.2:p.Ile196Ser
|
|
|
ENST00000462980.2:n.1177T>G
|
|
|
|
ENST00000472328.2:n.728T>G
|
|
|
|
ENST00000491610.2:n.622T>G
|
|
|
|
ENST00000676607.1:n.958T>G
|
|
|
|
ENST00000676627.1:n.1392T>G
|
|
|
|
ENST00000676708.1:n.1942T>G
|
|
|
|
ENST00000676864.1:n.1811T>G
|
|
|
|
ENST00000677010.1:c.698T>G
|
ENSP00000503089.1:p.Ile233Ser
|
|
|
ENST00000677108.1:n.2568T>G
|
|
|
|
ENST00000677168.1:n.1134T>G
|
|
|
|
ENST00000677185.1:n.1225T>G
|
|
|
|
ENST00000677205.1:n.1446T>G
|
|
|
|
ENST00000677344.1:n.1936T>G
|
|
|
|
ENST00000677480.1:c.*339T>G
|
ENSP00000504378.1:n.*339T>G
|
|
|
ENST00000677519.1:n.1372T>G
|
|
|
|
ENST00000677593.1:n.1218T>G
|
|
|
|
ENST00000677740.1:n.2167T>G
|
|
|
|
ENST00000677991.1:n.1835T>G
|
|
|
|
ENST00000678001.1:n.1155T>G
|
|
|
|
ENST00000678085.1:n.1218T>G
|
|
|
|
ENST00000678177.1:n.2511T>G
|
|
|
|
ENST00000678603.1:n.1740T>G
|
|
|
|
ENST00000678724.1:c.587T>G
|
ENSP00000503874.1:p.Ile196Ser
|
|
|
ENST00000678920.1:n.820T>G
|
|
|
|
ENST00000679019.1:n.1432T>G
|
|
|
|
ENST00000679117.1:c.*477T>G
|
ENSP00000503240.1:n.*477T>G
|
|
|
ENST00000679339.1:n.1503T>G
|
|
|
|
ENST00000326739.8:c.662T>G
|
ENSP00000321584.4:p.Ile221Ser
|
|
|
ENST00000429182.5:c.456T>G
|
|
|
|
ENST00000442157.1:c.587T>G
|
ENSP00000403502.1:p.Ile196Ser
|
|
|
ENST00000462980.1:n.564T>G
|
|
|
|
ENST00000491610.1:n.622T>G
|
|
|
|
NM_000884.2:c.662T>G
|
NP_000875.2:p.Ile221Ser
|
|
|
XM_006713128.2:c.872T>G
|
XP_006713191.1:p.Ile291Ser
|
|
|
XM_006713128.3:c.872T>G
|
XP_006713191.1:p.Ile291Ser
|
|
|
XM_017006349.1:c.797T>G
|
XP_016861838.1:p.Ile266Ser
|
|
|
XM_017006350.1:c.797T>G
|
XP_016861839.1:p.Ile266Ser
|
|
|
NM_000884.3:c.662T>G
MANE Select
|
NP_000875.2:p.Ile221Ser
|
|
