ENST00000646893.2:c.1037A>G
|
ENSP00000494249.2:p.Glu346Gly
|
|
ENST00000428343.6:c.698A>G
MANE Select
|
ENSP00000401536.1:p.Glu233Gly
|
|
ENST00000646446.1:c.911A>G
|
ENSP00000494216.1:p.Glu304Gly
|
|
ENST00000646893.1:c.824A>G
|
ENSP00000494249.1:p.Glu275Gly
|
|
ENST00000428343.5:c.698A>G
|
ENSP00000401536.1:p.Glu233Gly
|
|
ENST00000481179.5:c.*414A>G
|
ENSP00000422968.1:n.*414A>G
|
|
NM_001145664.1:c.698A>G
|
NP_001139136.1:p.Glu233Gly
|
|
XM_011511771.1:c.926A>G
|
XP_011510073.1:p.Glu309Gly
|
|
XM_011511772.1:c.911A>G
|
XP_011510074.1:p.Glu304Gly
|
|
XM_011511773.1:c.608A>G
|
XP_011510075.1:p.Glu203Gly
|
|
XM_011511774.1:c.926A>G
|
XP_011510076.1:p.Glu309Gly
|
|
XM_011511775.1:c.926A>G
|
XP_011510077.1:p.Glu309Gly
|
|
XM_011511776.1:c.410A>G
|
XP_011510078.1:p.Glu137Gly
|
|
XM_011511777.1:c.410A>G
|
XP_011510079.1:p.Glu137Gly
|
|
XM_011511778.1:c.410A>G
|
XP_011510080.1:p.Glu137Gly
|
|
XM_011511771.2:c.926A>G
|
XP_011510073.1:p.Glu309Gly
|
|
XM_011511777.2:c.410A>G
|
XP_011510079.1:p.Glu137Gly
|
|
XM_017004851.1:c.1037A>G
|
XP_016860340.1:p.Glu346Gly
|
|
XM_017004852.1:c.824A>G
|
XP_016860341.1:p.Glu275Gly
|
|
XM_017004853.1:c.1037A>G
|
XP_016860342.1:p.Glu346Gly
|
|
XM_017004854.1:c.1037A>G
|
XP_016860343.1:p.Glu346Gly
|
|
XR_001738924.1:n.981A>G
|
|
|
NM_001145664.2:c.698A>G
MANE Select
|
NP_001139136.2:p.Glu233Gly
|
|
NM_001367508.1:c.185A>G
|
NP_001354437.1:p.Glu62Gly
|
|
NM_001367509.1:c.185A>G
|
NP_001354438.1:p.Glu62Gly
|
|
NM_001367510.1:c.185A>G
|
NP_001354439.1:p.Glu62Gly
|
|