|
ENST00000703936.1:c.2749T>G
|
ENSP00000515567.1:p.Ser917Ala
|
|
|
ENST00000703937.1:c.*1810T>G
|
ENSP00000515568.1:n.*1810T>G
|
|
|
ENST00000326739.9:c.709T>G
MANE Select
|
ENSP00000321584.4:p.Ser237Ala
|
|
|
ENST00000429182.6:c.709T>G
|
ENSP00000393525.2:p.Ser237Ala
|
|
|
ENST00000442157.2:c.634T>G
|
ENSP00000403502.2:p.Ser212Ala
|
|
|
ENST00000462980.2:n.1224T>G
|
|
|
|
ENST00000472328.2:n.775T>G
|
|
|
|
ENST00000491610.2:n.669T>G
|
|
|
|
ENST00000676607.1:n.1005T>G
|
|
|
|
ENST00000676627.1:n.1439T>G
|
|
|
|
ENST00000676708.1:n.1989T>G
|
|
|
|
ENST00000676864.1:n.1858T>G
|
|
|
|
ENST00000677010.1:c.745T>G
|
ENSP00000503089.1:p.Ser249Ala
|
|
|
ENST00000677108.1:n.2615T>G
|
|
|
|
ENST00000677168.1:n.1181T>G
|
|
|
|
ENST00000677185.1:n.1272T>G
|
|
|
|
ENST00000677205.1:n.1493T>G
|
|
|
|
ENST00000677344.1:n.1983T>G
|
|
|
|
ENST00000677480.1:c.*386T>G
|
ENSP00000504378.1:n.*386T>G
|
|
|
ENST00000677519.1:n.1419T>G
|
|
|
|
ENST00000677593.1:n.1265T>G
|
|
|
|
ENST00000677740.1:n.2214T>G
|
|
|
|
ENST00000677991.1:n.1882T>G
|
|
|
|
ENST00000678001.1:n.1202T>G
|
|
|
|
ENST00000678085.1:n.1265T>G
|
|
|
|
ENST00000678177.1:n.2558T>G
|
|
|
|
ENST00000678603.1:n.1787T>G
|
|
|
|
ENST00000678724.1:c.634T>G
|
ENSP00000503874.1:p.Ser212Ala
|
|
|
ENST00000678920.1:n.867T>G
|
|
|
|
ENST00000679019.1:n.1479T>G
|
|
|
|
ENST00000679117.1:c.*524T>G
|
ENSP00000503240.1:n.*524T>G
|
|
|
ENST00000679339.1:n.1550T>G
|
|
|
|
ENST00000326739.8:c.709T>G
|
ENSP00000321584.4:p.Ser237Ala
|
|
|
ENST00000429182.5:c.503T>G
|
|
|
|
ENST00000442157.1:c.634T>G
|
ENSP00000403502.1:p.Ser212Ala
|
|
|
ENST00000462980.1:n.611T>G
|
|
|
|
ENST00000491610.1:n.669T>G
|
|
|
|
NM_000884.2:c.709T>G
|
NP_000875.2:p.Ser237Ala
|
|
|
XM_006713128.2:c.919T>G
|
XP_006713191.1:p.Ser307Ala
|
|
|
XM_006713128.3:c.919T>G
|
XP_006713191.1:p.Ser307Ala
|
|
|
XM_017006349.1:c.844T>G
|
XP_016861838.1:p.Ser282Ala
|
|
|
XM_017006350.1:c.844T>G
|
XP_016861839.1:p.Ser282Ala
|
|
|
NM_000884.3:c.709T>G
MANE Select
|
NP_000875.2:p.Ser237Ala
|
|
