|
NM_024426.6:c.1373G>A
MANE Select
|
NP_077744.4:p.Cys458Tyr
|
|
ENST00000452863.10:c.1373G>A
MANE Select
|
ENSP00000415516.5:p.Cys458Tyr
|
|
NM_000378.4:c.1307G>A
|
NP_000369.3:p.Cys436Tyr
|
|
NM_000378.5:c.1322G>A
|
NP_000369.4:p.Cys441Tyr
|
|
NM_000378.6:c.1322G>A
|
NP_000369.4:p.Cys441Tyr
|
|
NM_001198551.1:c.722G>A , LRG_525t2:c.722G>A
|
NP_001185480.1:p.Cys241Tyr
|
|
NM_001198552.1:c.671G>A
|
NP_001185481.1:p.Cys224Tyr
|
|
NM_001198552.2:c.671G>A
|
NP_001185481.1:p.Cys224Tyr
|
|
NM_001367854.1:c.185G>A
|
NP_001354783.1:p.Cys62Tyr
|
|
NM_024424.3:c.1358G>A
|
NP_077742.2:p.Cys453Tyr
|
|
NM_024424.4:c.1373G>A
|
NP_077742.3:p.Cys458Tyr
|
|
NM_024424.5:c.1373G>A
|
NP_077742.3:p.Cys458Tyr
|
|
NM_024426.4:c.1358G>A
|
NP_077744.3:p.Cys453Tyr
|
|
NM_024426.5:c.1373G>A
|
NP_077744.4:p.Cys458Tyr
|
|
NR_160306.1:n.1705G>A
|
|
|
ENST00000332351.7:c.1358G>A
|
ENSP00000331327.3:p.Cys453Tyr
|
|
ENST00000332351.9:c.1322G>A
|
ENSP00000331327.5:p.Cys441Tyr
|
|
ENST00000379077.7:c.*557G>A
|
ENSP00000368368.3:n.*557G>A
|
|
ENST00000379077.9:c.*557G>A
|
ENSP00000368368.5:n.*557G>A
|
|
ENST00000379079.6:c.722G>A
|
ENSP00000368370.2:p.Cys241Tyr
|
|
ENST00000379079.8:c.722G>A
|
ENSP00000368370.2:p.Cys241Tyr
|
|
ENST00000448076.7:c.1358G>A
|
ENSP00000413452.3:p.Cys453Tyr
|
|
ENST00000448076.9:c.1373G>A
|
ENSP00000413452.5:p.Cys458Tyr
|
|
ENST00000452863.7:c.1307G>A
|
ENSP00000415516.3:p.Cys436Tyr
|
|
ENST00000526685.2:n.827G>A
|
|
|
ENST00000527882.5:c.339G>A
|
|
|
ENST00000530998.5:c.671G>A
|
ENSP00000435307.1:p.Cys224Tyr
|
|
ENST00000639563.3:c.1322G>A
|
ENSP00000492269.3:p.Cys441Tyr
|
|
ENST00000639907.2:n.516G>A
|
|
|
ENST00000640146.2:c.698G>A
|
ENSP00000491984.2:p.Cys233Tyr
|
|
ENST00000650745.1:n.1183G>A
|
|
|
ENST00000650861.1:n.1954G>A
|
|
|
ENST00000650986.1:n.36G>A
|
|
|
ENST00000651459.1:c.144G>A
|
|
|
ENST00000651533.1:n.419G>A
|
|
|
ENST00000651668.1:n.310G>A
|
|
|
ENST00000651794.1:n.1216G>A
|
|
|
ENST00000651819.1:n.298G>A
|
|
|
ENST00000652579.1:n.633G>A
|
|
|
ENST00000652724.1:n.563G>A
|
|
