|
ENST00000332351.9:c.1214G=
|
ENSP00000331327.5:p.Gly405=
|
|
|
ENST00000379077.9:c.*449G=
|
ENSP00000368368.5:n.*449G=
|
|
|
ENST00000379079.8:c.614G=
|
ENSP00000368370.2:p.Gly205=
|
|
|
ENST00000448076.9:c.1265G=
|
ENSP00000413452.5:p.Gly422=
|
|
|
ENST00000452863.10:c.1265G=
MANE Select
|
ENSP00000415516.5:p.Gly422=
|
|
|
ENST00000526685.2:n.719G=
|
|
|
|
ENST00000639563.3:c.1214G=
|
ENSP00000492269.3:p.Gly405=
|
|
|
ENST00000639907.2:n.408G=
|
|
|
|
ENST00000640146.2:c.590G=
|
ENSP00000491984.2:p.Gly197=
|
|
|
ENST00000650745.1:n.474G=
|
|
|
|
ENST00000650861.1:n.1846G=
|
|
|
|
ENST00000651459.1:c.36G=
|
|
|
|
ENST00000651533.1:n.311G=
|
|
|
|
ENST00000651668.1:n.202G=
|
|
|
|
ENST00000651794.1:n.1108G=
|
|
|
|
ENST00000651819.1:n.190G=
|
|
|
|
ENST00000652579.1:n.525G=
|
|
|
|
ENST00000652724.1:n.455G=
|
|
|
|
ENST00000332351.7:c.1250G=
|
ENSP00000331327.3:p.Gly417=
|
|
|
ENST00000379077.7:c.*449G=
|
ENSP00000368368.3:n.*449G=
|
|
|
ENST00000379079.6:c.614G=
|
ENSP00000368370.2:p.Gly205=
|
|
|
ENST00000448076.7:c.1250G=
|
ENSP00000413452.3:p.Gly417=
|
|
|
ENST00000452863.7:c.1199G=
|
ENSP00000415516.3:p.Gly400=
|
|
|
ENST00000527882.5:c.321-691G=
|
|
|
|
ENST00000530998.5:c.563G=
|
ENSP00000435307.1:p.Gly188=
|
|
|
NM_000378.4:c.1199G=
|
NP_000369.3:p.Gly400=
|
|
|
NM_001198551.1:c.614G= , LRG_525t2:c.614G=
|
NP_001185480.1:p.Gly205=
|
|
|
NM_001198552.1:c.563G=
|
NP_001185481.1:p.Gly188=
|
|
|
NM_024424.3:c.1250G=
|
NP_077742.2:p.Gly417=
|
|
|
NM_024426.4:c.1250G=
|
NP_077744.3:p.Gly417=
|
|
|
NM_000378.5:c.1214G=
|
NP_000369.4:p.Gly405=
|
|
|
NM_024424.4:c.1265G=
|
NP_077742.3:p.Gly422=
|
|
|
NM_024426.5:c.1265G=
|
NP_077744.4:p.Gly422=
|
|
|
NM_001367854.1:c.77G=
|
NP_001354783.1:p.Gly26=
|
|
|
NR_160306.1:n.1597G=
|
|
|
|
NM_000378.6:c.1214G=
|
NP_000369.4:p.Gly405=
|
|
|
NM_001198552.2:c.563G=
|
NP_001185481.1:p.Gly188=
|
|
|
NM_024424.5:c.1265G=
|
NP_077742.3:p.Gly422=
|
|
|
NM_024426.6:c.1265G=
MANE Select
|
NP_077744.4:p.Gly422=
|
|
