|
ENST00000703936.1:c.2825T>C
|
ENSP00000515567.1:p.Leu942Ser
|
|
|
ENST00000703937.1:c.*1886T>C
|
ENSP00000515568.1:n.*1886T>C
|
|
|
ENST00000326739.9:c.785T>C
MANE Select
|
ENSP00000321584.4:p.Leu262Ser
|
|
|
ENST00000429182.6:c.785T>C
|
ENSP00000393525.2:p.Leu262Ser
|
|
|
ENST00000442157.2:c.710T>C
|
ENSP00000403502.2:p.Leu237Ser
|
|
|
ENST00000462980.2:n.1300T>C
|
|
|
|
ENST00000472328.2:n.851T>C
|
|
|
|
ENST00000491610.2:n.745T>C
|
|
|
|
ENST00000676607.1:n.1081T>C
|
|
|
|
ENST00000676627.1:n.1515T>C
|
|
|
|
ENST00000676708.1:n.2065T>C
|
|
|
|
ENST00000676864.1:n.1934T>C
|
|
|
|
ENST00000677010.1:c.821T>C
|
ENSP00000503089.1:p.Leu274Ser
|
|
|
ENST00000677108.1:n.2691T>C
|
|
|
|
ENST00000677168.1:n.1257T>C
|
|
|
|
ENST00000677185.1:n.1348T>C
|
|
|
|
ENST00000677205.1:n.1569T>C
|
|
|
|
ENST00000677344.1:n.2059T>C
|
|
|
|
ENST00000677480.1:c.*462T>C
|
ENSP00000504378.1:n.*462T>C
|
|
|
ENST00000677519.1:n.1495T>C
|
|
|
|
ENST00000677593.1:n.1341T>C
|
|
|
|
ENST00000677740.1:n.2290T>C
|
|
|
|
ENST00000677991.1:n.1958T>C
|
|
|
|
ENST00000678001.1:n.1278T>C
|
|
|
|
ENST00000678085.1:n.1341T>C
|
|
|
|
ENST00000678177.1:n.2634T>C
|
|
|
|
ENST00000678603.1:n.1863T>C
|
|
|
|
ENST00000678724.1:c.710T>C
|
ENSP00000503874.1:p.Leu237Ser
|
|
|
ENST00000678920.1:n.943T>C
|
|
|
|
ENST00000679019.1:n.1555T>C
|
|
|
|
ENST00000679117.1:c.*600T>C
|
ENSP00000503240.1:n.*600T>C
|
|
|
ENST00000679339.1:n.1626T>C
|
|
|
|
ENST00000326739.8:c.785T>C
|
ENSP00000321584.4:p.Leu262Ser
|
|
|
ENST00000429182.5:c.579T>C
|
|
|
|
ENST00000442157.1:c.710T>C
|
ENSP00000403502.1:p.Leu237Ser
|
|
|
ENST00000462980.1:n.687T>C
|
|
|
|
ENST00000491610.1:n.745T>C
|
|
|
|
NM_000884.2:c.785T>C
|
NP_000875.2:p.Leu262Ser
|
|
|
XM_006713128.2:c.995T>C
|
XP_006713191.1:p.Leu332Ser
|
|
|
XM_006713128.3:c.995T>C
|
XP_006713191.1:p.Leu332Ser
|
|
|
XM_017006349.1:c.920T>C
|
XP_016861838.1:p.Leu307Ser
|
|
|
XM_017006350.1:c.920T>C
|
XP_016861839.1:p.Leu307Ser
|
|
|
NM_000884.3:c.785T>C
MANE Select
|
NP_000875.2:p.Leu262Ser
|
|
