|
ENST00000703936.1:c.2705T>G
|
ENSP00000515567.1:p.Ile902Ser
|
|
|
ENST00000703937.1:c.*1766T>G
|
ENSP00000515568.1:n.*1766T>G
|
|
|
ENST00000326739.9:c.665T>G
MANE Select
|
ENSP00000321584.4:p.Ile222Ser
|
|
|
ENST00000429182.6:c.665T>G
|
ENSP00000393525.2:p.Ile222Ser
|
|
|
ENST00000442157.2:c.590T>G
|
ENSP00000403502.2:p.Ile197Ser
|
|
|
ENST00000462980.2:n.1180T>G
|
|
|
|
ENST00000472328.2:n.731T>G
|
|
|
|
ENST00000491610.2:n.625T>G
|
|
|
|
ENST00000676607.1:n.961T>G
|
|
|
|
ENST00000676627.1:n.1395T>G
|
|
|
|
ENST00000676708.1:n.1945T>G
|
|
|
|
ENST00000676864.1:n.1814T>G
|
|
|
|
ENST00000677010.1:c.701T>G
|
ENSP00000503089.1:p.Ile234Ser
|
|
|
ENST00000677108.1:n.2571T>G
|
|
|
|
ENST00000677168.1:n.1137T>G
|
|
|
|
ENST00000677185.1:n.1228T>G
|
|
|
|
ENST00000677205.1:n.1449T>G
|
|
|
|
ENST00000677344.1:n.1939T>G
|
|
|
|
ENST00000677480.1:c.*342T>G
|
ENSP00000504378.1:n.*342T>G
|
|
|
ENST00000677519.1:n.1375T>G
|
|
|
|
ENST00000677593.1:n.1221T>G
|
|
|
|
ENST00000677740.1:n.2170T>G
|
|
|
|
ENST00000677991.1:n.1838T>G
|
|
|
|
ENST00000678001.1:n.1158T>G
|
|
|
|
ENST00000678085.1:n.1221T>G
|
|
|
|
ENST00000678177.1:n.2514T>G
|
|
|
|
ENST00000678603.1:n.1743T>G
|
|
|
|
ENST00000678724.1:c.590T>G
|
ENSP00000503874.1:p.Ile197Ser
|
|
|
ENST00000678920.1:n.823T>G
|
|
|
|
ENST00000679019.1:n.1435T>G
|
|
|
|
ENST00000679117.1:c.*480T>G
|
ENSP00000503240.1:n.*480T>G
|
|
|
ENST00000679339.1:n.1506T>G
|
|
|
|
ENST00000326739.8:c.665T>G
|
ENSP00000321584.4:p.Ile222Ser
|
|
|
ENST00000429182.5:c.459T>G
|
|
|
|
ENST00000442157.1:c.590T>G
|
ENSP00000403502.1:p.Ile197Ser
|
|
|
ENST00000462980.1:n.567T>G
|
|
|
|
ENST00000491610.1:n.625T>G
|
|
|
|
NM_000884.2:c.665T>G
|
NP_000875.2:p.Ile222Ser
|
|
|
XM_006713128.2:c.875T>G
|
XP_006713191.1:p.Ile292Ser
|
|
|
XM_006713128.3:c.875T>G
|
XP_006713191.1:p.Ile292Ser
|
|
|
XM_017006349.1:c.800T>G
|
XP_016861838.1:p.Ile267Ser
|
|
|
XM_017006350.1:c.800T>G
|
XP_016861839.1:p.Ile267Ser
|
|
|
NM_000884.3:c.665T>G
MANE Select
|
NP_000875.2:p.Ile222Ser
|
|
