|
ENST00000332351.9:c.1293G=
|
ENSP00000331327.5:p.Arg431=
|
|
|
ENST00000379077.9:c.*528G=
|
ENSP00000368368.5:n.*528G=
|
|
|
ENST00000379079.8:c.693G=
|
ENSP00000368370.2:p.Arg231=
|
|
|
ENST00000448076.9:c.1344G=
|
ENSP00000413452.5:p.Arg448=
|
|
|
ENST00000452863.10:c.1344G=
MANE Select
|
ENSP00000415516.5:p.Arg448=
|
|
|
ENST00000526685.2:n.798G=
|
|
|
|
ENST00000639563.3:c.1293G=
|
ENSP00000492269.3:p.Arg431=
|
|
|
ENST00000639907.2:n.487G=
|
|
|
|
ENST00000640146.2:c.669G=
|
ENSP00000491984.2:p.Arg223=
|
|
|
ENST00000650745.1:n.553G=
|
|
|
|
ENST00000650861.1:n.1925G=
|
|
|
|
ENST00000651459.1:c.115G=
|
|
|
|
ENST00000651533.1:n.390G=
|
|
|
|
ENST00000651668.1:n.281G=
|
|
|
|
ENST00000651794.1:n.1187G=
|
|
|
|
ENST00000651819.1:n.269G=
|
|
|
|
ENST00000652579.1:n.604G=
|
|
|
|
ENST00000652724.1:n.534G=
|
|
|
|
ENST00000332351.7:c.1329G=
|
ENSP00000331327.3:p.Arg443=
|
|
|
ENST00000379077.7:c.*528G=
|
ENSP00000368368.3:n.*528G=
|
|
|
ENST00000379079.6:c.693G=
|
ENSP00000368370.2:p.Arg231=
|
|
|
ENST00000448076.7:c.1329G=
|
ENSP00000413452.3:p.Arg443=
|
|
|
ENST00000452863.7:c.1278G=
|
ENSP00000415516.3:p.Arg426=
|
|
|
ENST00000527882.5:c.321-612G=
|
|
|
|
ENST00000530998.5:c.642G=
|
ENSP00000435307.1:p.Arg214=
|
|
|
NM_000378.4:c.1278G=
|
NP_000369.3:p.Arg426=
|
|
|
NM_001198551.1:c.693G= , LRG_525t2:c.693G=
|
NP_001185480.1:p.Arg231=
|
|
|
NM_001198552.1:c.642G=
|
NP_001185481.1:p.Arg214=
|
|
|
NM_024424.3:c.1329G=
|
NP_077742.2:p.Arg443=
|
|
|
NM_024426.4:c.1329G=
|
NP_077744.3:p.Arg443=
|
|
|
NM_000378.5:c.1293G=
|
NP_000369.4:p.Arg431=
|
|
|
NM_024424.4:c.1344G=
|
NP_077742.3:p.Arg448=
|
|
|
NM_024426.5:c.1344G=
|
NP_077744.4:p.Arg448=
|
|
|
NM_001367854.1:c.156G=
|
NP_001354783.1:p.Arg52=
|
|
|
NR_160306.1:n.1676G=
|
|
|
|
NM_000378.6:c.1293G=
|
NP_000369.4:p.Arg431=
|
|
|
NM_001198552.2:c.642G=
|
NP_001185481.1:p.Arg214=
|
|
|
NM_024424.5:c.1344G=
|
NP_077742.3:p.Arg448=
|
|
|
NM_024426.6:c.1344G=
MANE Select
|
NP_077744.4:p.Arg448=
|
|
