|
ENST00000332351.9:c.1349G=
|
ENSP00000331327.5:p.Arg450=
|
|
|
ENST00000379077.9:c.*584G=
|
ENSP00000368368.5:n.*584G=
|
|
|
ENST00000379079.8:c.749G=
|
ENSP00000368370.2:p.Arg250=
|
|
|
ENST00000448076.9:c.1400G=
|
ENSP00000413452.5:p.Arg467=
|
|
|
ENST00000452863.10:c.1400G=
MANE Select
|
ENSP00000415516.5:p.Arg467=
|
|
|
ENST00000526685.2:n.854G=
|
|
|
|
ENST00000639563.3:c.1349G=
|
ENSP00000492269.3:p.Arg450=
|
|
|
ENST00000639907.2:n.543G=
|
|
|
|
ENST00000640146.2:c.725G=
|
ENSP00000491984.2:p.Arg242=
|
|
|
ENST00000650745.1:n.1210G=
|
|
|
|
ENST00000650861.1:n.1981G=
|
|
|
|
ENST00000650986.1:n.63G=
|
|
|
|
ENST00000651459.1:c.171G=
|
|
|
|
ENST00000651533.1:n.446G=
|
|
|
|
ENST00000651668.1:n.337G=
|
|
|
|
ENST00000651794.1:n.1243G=
|
|
|
|
ENST00000651819.1:n.325G=
|
|
|
|
ENST00000652579.1:n.660G=
|
|
|
|
ENST00000652724.1:n.590G=
|
|
|
|
ENST00000332351.7:c.1385G=
|
ENSP00000331327.3:p.Arg462=
|
|
|
ENST00000379077.7:c.*584G=
|
ENSP00000368368.3:n.*584G=
|
|
|
ENST00000379079.6:c.749G=
|
ENSP00000368370.2:p.Arg250=
|
|
|
ENST00000448076.7:c.1385G=
|
ENSP00000413452.3:p.Arg462=
|
|
|
ENST00000452863.7:c.1334G=
|
ENSP00000415516.3:p.Arg445=
|
|
|
ENST00000527882.5:c.366G=
|
|
|
|
ENST00000530998.5:c.698G=
|
ENSP00000435307.1:p.Arg233=
|
|
|
NM_000378.4:c.1334G=
|
NP_000369.3:p.Arg445=
|
|
|
NM_001198551.1:c.749G= , LRG_525t2:c.749G=
|
NP_001185480.1:p.Arg250=
|
|
|
NM_001198552.1:c.698G=
|
NP_001185481.1:p.Arg233=
|
|
|
NM_024424.3:c.1385G=
|
NP_077742.2:p.Arg462=
|
|
|
NM_024426.4:c.1385G=
|
NP_077744.3:p.Arg462=
|
|
|
NM_000378.5:c.1349G=
|
NP_000369.4:p.Arg450=
|
|
|
NM_024424.4:c.1400G=
|
NP_077742.3:p.Arg467=
|
|
|
NM_024426.5:c.1400G=
|
NP_077744.4:p.Arg467=
|
|
|
NM_001367854.1:c.212G=
|
NP_001354783.1:p.Arg71=
|
|
|
NR_160306.1:n.1732G=
|
|
|
|
NM_000378.6:c.1349G=
|
NP_000369.4:p.Arg450=
|
|
|
NM_001198552.2:c.698G=
|
NP_001185481.1:p.Arg233=
|
|
|
NM_024424.5:c.1400G=
|
NP_077742.3:p.Arg467=
|
|
|
NM_024426.6:c.1400G=
MANE Select
|
NP_077744.4:p.Arg467=
|
|
