|
NM_024426.6:c.1253G>T
MANE Select
|
NP_077744.4:p.Arg418Met
|
|
ENST00000452863.10:c.1253G>T
MANE Select
|
ENSP00000415516.5:p.Arg418Met
|
|
NM_000378.4:c.1187G>T
|
NP_000369.3:p.Arg396Met
|
|
NM_000378.5:c.1202G>T
|
NP_000369.4:p.Arg401Met
|
|
NM_000378.6:c.1202G>T
|
NP_000369.4:p.Arg401Met
|
|
NM_001198551.1:c.602G>T , LRG_525t2:c.602G>T
|
NP_001185480.1:p.Arg201Met
|
|
NM_001198552.1:c.551G>T
|
NP_001185481.1:p.Arg184Met
|
|
NM_001198552.2:c.551G>T
|
NP_001185481.1:p.Arg184Met
|
|
NM_001367854.1:c.65G>T
|
NP_001354783.1:p.Arg22Met
|
|
NM_024424.3:c.1238G>T
|
NP_077742.2:p.Arg413Met
|
|
NM_024424.4:c.1253G>T
|
NP_077742.3:p.Arg418Met
|
|
NM_024424.5:c.1253G>T
|
NP_077742.3:p.Arg418Met
|
|
NM_024426.4:c.1238G>T
|
NP_077744.3:p.Arg413Met
|
|
NM_024426.5:c.1253G>T
|
NP_077744.4:p.Arg418Met
|
|
NR_160306.1:n.1585G>T
|
|
|
ENST00000332351.7:c.1238G>T
|
ENSP00000331327.3:p.Arg413Met
|
|
ENST00000332351.9:c.1202G>T
|
ENSP00000331327.5:p.Arg401Met
|
|
ENST00000379077.7:c.*437G>T
|
ENSP00000368368.3:n.*437G>T
|
|
ENST00000379077.9:c.*437G>T
|
ENSP00000368368.5:n.*437G>T
|
|
ENST00000379079.6:c.602G>T
|
ENSP00000368370.2:p.Arg201Met
|
|
ENST00000379079.8:c.602G>T
|
ENSP00000368370.2:p.Arg201Met
|
|
ENST00000448076.7:c.1238G>T
|
ENSP00000413452.3:p.Arg413Met
|
|
ENST00000448076.9:c.1253G>T
|
ENSP00000413452.5:p.Arg418Met
|
|
ENST00000452863.7:c.1187G>T
|
ENSP00000415516.3:p.Arg396Met
|
|
ENST00000526685.1:c.65G>T
|
ENSP00000436292.1:p.Arg22Met
|
|
ENST00000526685.2:n.707G>T
|
|
|
ENST00000527882.5:c.309G>T
|
|
|
ENST00000530998.5:c.551G>T
|
ENSP00000435307.1:p.Arg184Met
|
|
ENST00000639563.3:c.1202G>T
|
ENSP00000492269.3:p.Arg401Met
|
|
ENST00000639907.2:n.396G>T
|
|
|
ENST00000640146.2:c.578G>T
|
ENSP00000491984.2:p.Arg193Met
|
|
ENST00000650861.1:n.1834G>T
|
|
|
ENST00000651459.1:c.36-3513G>T
|
|
|
ENST00000651668.1:n.190G>T
|
|
|
ENST00000651794.1:n.996G>T
|
|
|
ENST00000651819.1:n.178G>T
|
|
|
ENST00000652579.1:n.413G>T
|
|
|
ENST00000652724.1:n.443G>T
|
|
