ENST00000332351.9:c.1478G>C
|
ENSP00000331327.5:p.Arg493Thr
|
|
ENST00000379077.9:c.*722G>C
|
ENSP00000368368.5:n.*722G>C
|
|
ENST00000379079.8:c.878G>C
|
ENSP00000368370.2:p.Arg293Thr
|
|
ENST00000448076.9:c.1529G>C
|
ENSP00000413452.5:p.Arg510Thr
|
|
ENST00000452863.10:c.1538G>C
MANE Select
|
ENSP00000415516.5:p.Arg513Thr
|
|
ENST00000639563.3:c.1487G>C
|
ENSP00000492269.3:p.Arg496Thr
|
|
ENST00000639907.2:n.672G>C
|
|
|
ENST00000640146.2:c.863G>C
|
ENSP00000491984.2:p.Arg288Thr
|
|
ENST00000650745.1:n.1348G>C
|
|
|
ENST00000650861.1:n.2110G>C
|
|
|
ENST00000650986.1:n.201G>C
|
|
|
ENST00000651459.1:c.309G>C
|
|
|
ENST00000651533.1:n.575G>C
|
|
|
ENST00000651668.1:n.475G>C
|
|
|
ENST00000651794.1:n.1381G>C
|
|
|
ENST00000651819.1:n.463G>C
|
|
|
ENST00000652579.1:n.798G>C
|
|
|
ENST00000652724.1:n.728G>C
|
|
|
ENST00000332351.7:c.1523G>C
|
ENSP00000331327.3:p.Arg508Thr
|
|
ENST00000379077.7:c.*722G>C
|
ENSP00000368368.3:n.*722G>C
|
|
ENST00000379079.6:c.878G>C
|
ENSP00000368370.2:p.Arg293Thr
|
|
ENST00000448076.7:c.1514G>C
|
ENSP00000413452.3:p.Arg505Thr
|
|
ENST00000452863.7:c.1463G>C
|
ENSP00000415516.3:p.Arg488Thr
|
|
ENST00000527882.5:c.504G>C
|
|
|
ENST00000530998.5:c.836G>C
|
ENSP00000435307.1:p.Arg279Thr
|
|
NM_000378.4:c.1463G>C
|
NP_000369.3:p.Arg488Thr
|
|
NM_001198551.1:c.878G>C , LRG_525t2:c.878G>C
|
NP_001185480.1:p.Arg293Thr
|
|
NM_001198552.1:c.836G>C
|
NP_001185481.1:p.Arg279Thr
|
|
NM_024424.3:c.1514G>C
|
NP_077742.2:p.Arg505Thr
|
|
NM_024426.4:c.1523G>C
|
NP_077744.3:p.Arg508Thr
|
|
NM_000378.5:c.1478G>C
|
NP_000369.4:p.Arg493Thr
|
|
NM_024424.4:c.1529G>C
|
NP_077742.3:p.Arg510Thr
|
|
NM_024426.5:c.1538G>C
|
NP_077744.4:p.Arg513Thr
|
|
NM_001367854.1:c.350G>C
|
NP_001354783.1:p.Arg117Thr
|
|
NR_160306.1:n.1870G>C
|
|
|
NM_000378.6:c.1478G>C
|
NP_000369.4:p.Arg493Thr
|
|
NM_001198552.2:c.836G>C
|
NP_001185481.1:p.Arg279Thr
|
|
NM_024424.5:c.1529G>C
|
NP_077742.3:p.Arg510Thr
|
|
NM_024426.6:c.1538G>C
MANE Select
|
NP_077744.4:p.Arg513Thr
|
|