|
ENST00000700029.2:c.1076C>G
|
ENSP00000514759.2:p.Ala359Gly
|
|
|
ENST00000710265.1:c.983C>G
|
ENSP00000518161.1:p.Ala328Gly
|
|
|
ENST00000472832.3:c.983C>G
|
ENSP00000483066.2:p.Ala328Gly
|
|
|
ENST00000688158.2:n.1718C>G
|
|
|
|
ENST00000688922.2:c.*813C>G
|
ENSP00000508742.2:n.*813C>G
|
|
|
ENST00000700021.1:c.938C>G
|
ENSP00000514757.1:p.Ala313Gly
|
|
|
ENST00000700022.1:c.*322C>G
|
ENSP00000514758.1:n.*322C>G
|
|
|
ENST00000700023.1:n.2141C>G
|
|
|
|
ENST00000700024.1:n.2375C>G
|
|
|
|
ENST00000700025.1:n.1752C>G
|
|
|
|
ENST00000700026.1:n.620C>G
|
|
|
|
ENST00000706954.1:c.983C>G
|
ENSP00000516674.1:p.Ala328Gly
|
|
|
ENST00000706955.1:c.*1018C>G
|
ENSP00000516675.1:n.*1018C>G
|
|
|
ENST00000686459.1:c.*569C>G
|
ENSP00000508909.1:n.*569C>G
|
|
|
ENST00000688158.1:c.*1094C>G
|
ENSP00000509254.1:n.*1094C>G
|
|
|
ENST00000688308.1:c.983C>G
|
ENSP00000508752.1:p.Ala328Gly
|
|
|
ENST00000688922.1:c.904C>G
|
|
|
|
ENST00000693560.1:c.1502C>G
|
ENSP00000509861.1:p.Ala501Gly
|
|
|
ENST00000371953.8:c.983C>G
MANE Select
|
ENSP00000361021.3:p.Ala328Gly
|
|
|
ENST00000371953.7:c.983C>G
|
ENSP00000361021.3:p.Ala328Gly
|
|
|
ENST00000472832.2:c.410C>G
|
ENSP00000483066.1:p.Ala137Gly
|
|
|
NM_000314.5:c.983C>G
|
NP_000305.3:p.Ala328Gly
|
|
|
NM_000314.6:c.983C>G
|
NP_000305.3:p.Ala328Gly
|
|
|
NM_001304717.2:c.1502C>G
|
NP_001291646.2:p.Ala501Gly
|
|
|
NM_001304718.1:c.392C>G
|
NP_001291647.1:p.Ala131Gly
|
|
|
XM_006717926.2:c.938C>G
|
XP_006717989.1:p.Ala313Gly
|
|
|
XM_011539981.1:c.983C>G
|
XP_011538283.1:p.Ala328Gly
|
|
|
XM_011539982.1:c.887C>G
|
XP_011538284.1:p.Ala296Gly
|
|
|
XR_945791.1:n.1553C>G
|
|
|
|
NM_000314.7:c.983C>G
|
NP_000305.3:p.Ala328Gly
|
|
|
NM_001304717.5:c.1502C>G
|
NP_001291646.4:p.Ala501Gly
|
|
|
NM_001304718.2:c.392C>G
|
NP_001291647.1:p.Ala131Gly
|
|
|
NM_000314.8:c.983C>G
MANE Select
|
NP_000305.3:p.Ala328Gly
|
|
