|
ENST00000332351.9:c.1296A>G
|
ENSP00000331327.5:p.Arg432=
|
|
|
ENST00000379077.9:c.*531A>G
|
ENSP00000368368.5:n.*531A>G
|
|
|
ENST00000379079.8:c.696A>G
|
ENSP00000368370.2:p.Arg232=
|
|
|
ENST00000448076.9:c.1347A>G
|
ENSP00000413452.5:p.Arg449=
|
|
|
ENST00000452863.10:c.1347A>G
MANE Select
|
ENSP00000415516.5:p.Arg449=
|
|
|
ENST00000526685.2:n.801A>G
|
|
|
|
ENST00000639563.3:c.1296A>G
|
ENSP00000492269.3:p.Arg432=
|
|
|
ENST00000639907.2:n.490A>G
|
|
|
|
ENST00000640146.2:c.672A>G
|
ENSP00000491984.2:p.Arg224=
|
|
|
ENST00000650745.1:n.556A>G
|
|
|
|
ENST00000650861.1:n.1928A>G
|
|
|
|
ENST00000651459.1:c.118A>G
|
|
|
|
ENST00000651533.1:n.393A>G
|
|
|
|
ENST00000651668.1:n.284A>G
|
|
|
|
ENST00000651794.1:n.1190A>G
|
|
|
|
ENST00000651819.1:n.272A>G
|
|
|
|
ENST00000652579.1:n.607A>G
|
|
|
|
ENST00000652724.1:n.537A>G
|
|
|
|
ENST00000332351.7:c.1332A>G
|
ENSP00000331327.3:p.Arg444=
|
|
|
ENST00000379077.7:c.*531A>G
|
ENSP00000368368.3:n.*531A>G
|
|
|
ENST00000379079.6:c.696A>G
|
ENSP00000368370.2:p.Arg232=
|
|
|
ENST00000448076.7:c.1332A>G
|
ENSP00000413452.3:p.Arg444=
|
|
|
ENST00000452863.7:c.1281A>G
|
ENSP00000415516.3:p.Arg427=
|
|
|
ENST00000527882.5:c.321-609A>G
|
|
|
|
ENST00000530998.5:c.645A>G
|
ENSP00000435307.1:p.Arg215=
|
|
|
NM_000378.4:c.1281A>G
|
NP_000369.3:p.Arg427=
|
|
|
NM_001198551.1:c.696A>G , LRG_525t2:c.696A>G
|
NP_001185480.1:p.Arg232=
|
|
|
NM_001198552.1:c.645A>G
|
NP_001185481.1:p.Arg215=
|
|
|
NM_024424.3:c.1332A>G
|
NP_077742.2:p.Arg444=
|
|
|
NM_024426.4:c.1332A>G
|
NP_077744.3:p.Arg444=
|
|
|
NM_000378.5:c.1296A>G
|
NP_000369.4:p.Arg432=
|
|
|
NM_024424.4:c.1347A>G
|
NP_077742.3:p.Arg449=
|
|
|
NM_024426.5:c.1347A>G
|
NP_077744.4:p.Arg449=
|
|
|
NM_001367854.1:c.159A>G
|
NP_001354783.1:p.Arg53=
|
|
|
NR_160306.1:n.1679A>G
|
|
|
|
NM_000378.6:c.1296A>G
|
NP_000369.4:p.Arg432=
|
|
|
NM_001198552.2:c.645A>G
|
NP_001185481.1:p.Arg215=
|
|
|
NM_024424.5:c.1347A>G
|
NP_077742.3:p.Arg449=
|
|
|
NM_024426.6:c.1347A>G
MANE Select
|
NP_077744.4:p.Arg449=
|
|
