|
NM_024426.6:c.1498C>T
MANE Select
|
NP_077744.4:p.Arg500Trp
|
|
ENST00000452863.10:c.1498C>T
MANE Select
|
ENSP00000415516.5:p.Arg500Trp
|
|
NM_000378.4:c.1423C>T
|
NP_000369.3:p.Arg475Trp
|
|
NM_000378.5:c.1438C>T
|
NP_000369.4:p.Arg480Trp
|
|
NM_000378.6:c.1438C>T
|
NP_000369.4:p.Arg480Trp
|
|
NM_001198551.1:c.838C>T , LRG_525t2:c.838C>T
|
NP_001185480.1:p.Arg280Trp
|
|
NM_001198552.1:c.796C>T
|
NP_001185481.1:p.Arg266Trp
|
|
NM_001198552.2:c.796C>T
|
NP_001185481.1:p.Arg266Trp
|
|
NM_001367854.1:c.310C>T
|
NP_001354783.1:p.Arg104Trp
|
|
NM_024424.3:c.1474C>T
|
NP_077742.2:p.Arg492Trp
|
|
NM_024424.4:c.1489C>T
|
NP_077742.3:p.Arg497Trp
|
|
NM_024424.5:c.1489C>T
|
NP_077742.3:p.Arg497Trp
|
|
NM_024426.4:c.1483C>T
|
NP_077744.3:p.Arg495Trp
|
|
NM_024426.5:c.1498C>T
|
NP_077744.4:p.Arg500Trp
|
|
NR_160306.1:n.1830C>T
|
|
|
ENST00000332351.7:c.1483C>T
|
ENSP00000331327.3:p.Arg495Trp
|
|
ENST00000332351.9:c.1438C>T
|
ENSP00000331327.5:p.Arg480Trp
|
|
ENST00000379077.7:c.*682C>T
|
ENSP00000368368.3:n.*682C>T
|
|
ENST00000379077.9:c.*682C>T
|
ENSP00000368368.5:n.*682C>T
|
|
ENST00000379079.6:c.838C>T
|
ENSP00000368370.2:p.Arg280Trp
|
|
ENST00000379079.8:c.838C>T
|
ENSP00000368370.2:p.Arg280Trp
|
|
ENST00000448076.7:c.1474C>T
|
ENSP00000413452.3:p.Arg492Trp
|
|
ENST00000448076.9:c.1489C>T
|
ENSP00000413452.5:p.Arg497Trp
|
|
ENST00000452863.7:c.1423C>T
|
ENSP00000415516.3:p.Arg475Trp
|
|
ENST00000526685.2:n.943C>T
|
|
|
ENST00000527882.5:c.464C>T
|
|
|
ENST00000530998.5:c.796C>T
|
ENSP00000435307.1:p.Arg266Trp
|
|
ENST00000639563.3:c.1447C>T
|
ENSP00000492269.3:p.Arg483Trp
|
|
ENST00000639907.2:n.632C>T
|
|
|
ENST00000640146.2:c.823C>T
|
ENSP00000491984.2:p.Arg275Trp
|
|
ENST00000650745.1:n.1308C>T
|
|
|
ENST00000650861.1:n.2070C>T
|
|
|
ENST00000650986.1:n.161C>T
|
|
|
ENST00000651459.1:c.269C>T
|
|
|
ENST00000651533.1:n.535C>T
|
|
|
ENST00000651668.1:n.435C>T
|
|
|
ENST00000651794.1:n.1341C>T
|
|
|
ENST00000651819.1:n.423C>T
|
|
|
ENST00000652579.1:n.758C>T
|
|
|
ENST00000652724.1:n.688C>T
|
|
