ENST00000321264.9:c.1421C>G
MANE Select
|
ENSP00000315351.4:p.Ala474Gly
|
|
ENST00000321264.8:c.1421C>G
|
ENSP00000315351.4:p.Ala474Gly
|
|
ENST00000400769.6:c.*171C>G
|
ENSP00000383580.2:n.*171C>G
|
|
ENST00000403782.5:c.1019C>G
|
ENSP00000384723.1:p.Ala340Gly
|
|
ENST00000436747.5:c.*2657C>G
|
ENSP00000400212.1:n.*2657C>G
|
|
ENST00000445308.1:c.817C>G
|
|
|
ENST00000468064.5:n.1311C>G
|
|
|
ENST00000470343.5:n.902C>G
|
|
|
ENST00000473126.1:n.620C>G
|
|
|
ENST00000486953.5:n.1245C>G
|
|
|
ENST00000610344.1:c.*265C>G
|
ENSP00000481906.1:n.*265C>G
|
|
NM_001287249.1:c.1019C>G
|
NP_001274178.1:p.Ala340Gly
|
|
NM_152783.4:c.1421C>G
|
NP_689996.4:p.Ala474Gly
|
|
NR_109778.1:n.1343C>G
|
|
|
XM_011511734.1:c.1541C>G
|
XP_011510036.1:p.Ala514Gly
|
|
XM_011511735.1:c.1499C>G
|
XP_011510037.1:p.Ala500Gly
|
|
XM_011511736.1:c.1463C>G
|
XP_011510038.1:p.Ala488Gly
|
|
XM_011511750.1:c.*88C>G
|
XP_011510052.1:n.*88C>G
|
|
XM_011511754.1:c.980C>G
|
XP_011510056.1:p.Ala327Gly
|
|
XM_011511755.1:c.971C>G
|
XP_011510057.1:p.Ala324Gly
|
|
XM_011511756.1:c.968C>G
|
XP_011510058.1:p.Ala323Gly
|
|
XR_923004.1:n.2053C>G
|
|
|
XR_923007.1:n.1763C>G
|
|
|
XR_923011.1:n.1864C>G
|
|
|
NM_001352824.1:c.860C>G
|
NP_001339753.1:p.Ala287Gly
|
|
XM_011511734.2:c.1541C>G
|
XP_011510036.1:p.Ala514Gly
|
|
XM_011511735.2:c.1499C>G
|
XP_011510037.1:p.Ala500Gly
|
|
XM_011511736.2:c.1463C>G
|
XP_011510038.1:p.Ala488Gly
|
|
XM_011511750.3:c.*88C>G
|
XP_011510052.1:n.*88C>G
|
|
XM_011511756.2:c.968C>G
|
XP_011510058.1:p.Ala323Gly
|
|
XM_024453102.1:c.1313C>G
|
XP_024308870.1:p.Ala438Gly
|
|
XR_001738918.2:n.1795C>G
|
|
|
XR_001738919.2:n.1729C>G
|
|
|
XR_923004.3:n.2052C>G
|
|
|
XR_923007.3:n.1762C>G
|
|
|
XR_923011.3:n.1863C>G
|
|
|
NM_152783.5:c.1421C>G
MANE Select
|
NP_689996.4:p.Ala474Gly
|
|
NM_001287249.2:c.1019C>G
|
NP_001274178.1:p.Ala340Gly
|
|
NM_001352824.2:c.860C>G
|
NP_001339753.1:p.Ala287Gly
|
|
NR_109778.2:n.1292C>G
|
|
|