|
ENST00000703936.1:c.2831C>G
|
ENSP00000515567.1:p.Ala944Gly
|
|
|
ENST00000703937.1:c.*1892C>G
|
ENSP00000515568.1:n.*1892C>G
|
|
|
ENST00000326739.9:c.791C>G
MANE Select
|
ENSP00000321584.4:p.Ala264Gly
|
|
|
ENST00000429182.6:c.791C>G
|
ENSP00000393525.2:p.Ala264Gly
|
|
|
ENST00000442157.2:c.716C>G
|
ENSP00000403502.2:p.Ala239Gly
|
|
|
ENST00000462980.2:n.1306C>G
|
|
|
|
ENST00000472328.2:n.857C>G
|
|
|
|
ENST00000491610.2:n.751C>G
|
|
|
|
ENST00000676607.1:n.1087C>G
|
|
|
|
ENST00000676627.1:n.1521C>G
|
|
|
|
ENST00000676708.1:n.2071C>G
|
|
|
|
ENST00000676864.1:n.1940C>G
|
|
|
|
ENST00000677010.1:c.827C>G
|
ENSP00000503089.1:p.Ala276Gly
|
|
|
ENST00000677108.1:n.2697C>G
|
|
|
|
ENST00000677168.1:n.1263C>G
|
|
|
|
ENST00000677185.1:n.1354C>G
|
|
|
|
ENST00000677205.1:n.1575C>G
|
|
|
|
ENST00000677344.1:n.2065C>G
|
|
|
|
ENST00000677480.1:c.*468C>G
|
ENSP00000504378.1:n.*468C>G
|
|
|
ENST00000677519.1:n.1501C>G
|
|
|
|
ENST00000677593.1:n.1347C>G
|
|
|
|
ENST00000677740.1:n.2296C>G
|
|
|
|
ENST00000677991.1:n.1964C>G
|
|
|
|
ENST00000678001.1:n.1284C>G
|
|
|
|
ENST00000678085.1:n.1347C>G
|
|
|
|
ENST00000678177.1:n.2640C>G
|
|
|
|
ENST00000678603.1:n.1869C>G
|
|
|
|
ENST00000678724.1:c.716C>G
|
ENSP00000503874.1:p.Ala239Gly
|
|
|
ENST00000678920.1:n.949C>G
|
|
|
|
ENST00000679019.1:n.1561C>G
|
|
|
|
ENST00000679117.1:c.*606C>G
|
ENSP00000503240.1:n.*606C>G
|
|
|
ENST00000679339.1:n.1632C>G
|
|
|
|
ENST00000326739.8:c.791C>G
|
ENSP00000321584.4:p.Ala264Gly
|
|
|
ENST00000429182.5:c.585C>G
|
|
|
|
ENST00000442157.1:c.716C>G
|
ENSP00000403502.1:p.Ala239Gly
|
|
|
ENST00000462980.1:n.693C>G
|
|
|
|
ENST00000491610.1:n.751C>G
|
|
|
|
NM_000884.2:c.791C>G
|
NP_000875.2:p.Ala264Gly
|
|
|
XM_006713128.2:c.1001C>G
|
XP_006713191.1:p.Ala334Gly
|
|
|
XM_006713128.3:c.1001C>G
|
XP_006713191.1:p.Ala334Gly
|
|
|
XM_017006349.1:c.926C>G
|
XP_016861838.1:p.Ala309Gly
|
|
|
XM_017006350.1:c.926C>G
|
XP_016861839.1:p.Ala309Gly
|
|
|
NM_000884.3:c.791C>G
MANE Select
|
NP_000875.2:p.Ala264Gly
|
|
