ENST00000698724.1:n.1855A>G
|
|
|
ENST00000698725.1:n.1608A>G
|
|
|
ENST00000698726.1:n.3168A>G
|
|
|
ENST00000698727.1:n.2901A>G
|
|
|
ENST00000698728.1:n.3517A>G
|
|
|
ENST00000698729.1:n.4965A>G
|
|
|
ENST00000698730.1:n.5063A>G
|
|
|
ENST00000698731.1:c.3797A>G
|
ENSP00000513898.1:p.Glu1266Gly
|
|
ENST00000698732.1:c.*2627A>G
|
ENSP00000513899.1:n.*2627A>G
|
|
ENST00000698733.1:c.*3125A>G
|
ENSP00000513900.1:n.*3125A>G
|
|
ENST00000698734.1:c.*2111A>G
|
ENSP00000513901.1:n.*2111A>G
|
|
ENST00000698735.1:n.4289A>G
|
|
|
ENST00000698736.1:n.4702A>G
|
|
|
ENST00000698737.1:n.4053A>G
|
|
|
ENST00000372371.8:c.3938A>G
MANE Select
|
ENSP00000361446.3:p.Glu1313Gly
|
|
ENST00000372371.7:c.3938A>G
|
ENSP00000361446.3:p.Glu1313Gly
|
|
ENST00000616246.4:c.386A>G
|
ENSP00000483738.1:p.Glu129Gly
|
|
NM_007055.3:c.3938A>G
|
NP_008986.2:p.Glu1313Gly
|
|
NM_007055.4:c.3938A>G
MANE Select
|
NP_008986.2:p.Glu1313Gly
|
|