ENST00000332351.9:c.*685G>T
|
ENSP00000331327.5:n.*685G>T
|
|
ENST00000379077.9:c.*1438G>T
|
ENSP00000368368.5:n.*1438G>T
|
|
ENST00000379079.8:c.*685G>T
|
ENSP00000368370.2:n.*685G>T
|
|
ENST00000452863.10:c.*685G>T
MANE Select
|
ENSP00000415516.5:n.*685G>T
|
|
ENST00000639907.2:n.1388G>T
|
|
|
ENST00000640146.2:c.*685G>T
|
ENSP00000491984.2:n.*685G>T
|
|
ENST00000650745.1:n.2064G>T
|
|
|
ENST00000650861.1:n.2826G>T
|
|
|
ENST00000651459.1:c.1025G>T
|
|
|
ENST00000651533.1:n.1291G>T
|
|
|
ENST00000651668.1:n.1191G>T
|
|
|
ENST00000651794.1:n.2097G>T
|
|
|
ENST00000651819.1:n.1179G>T
|
|
|
ENST00000652579.1:n.1514G>T
|
|
|
ENST00000652724.1:n.1444G>T
|
|
|
ENST00000332351.7:c.*685G>T
|
ENSP00000331327.3:n.*685G>T
|
|
ENST00000379077.7:c.*1438G>T
|
ENSP00000368368.3:n.*1438G>T
|
|
ENST00000379079.6:c.*685G>T
|
ENSP00000368370.2:n.*685G>T
|
|
ENST00000452863.7:c.2179G>T
|
ENSP00000415516.3:n.2179G>T
|
|
ENST00000530998.5:c.*685G>T
|
ENSP00000435307.1:n.*685G>T
|
|
NM_000378.4:c.*685G>T
|
NP_000369.3:n.*685G>T
|
|
NM_001198551.1:c.*685G>T , LRG_525t2:c.*685G>T
|
NP_001185480.1:n.*685G>T
|
|
NM_001198552.1:c.*685G>T
|
NP_001185481.1:n.*685G>T
|
|
NM_024424.3:c.*685G>T
|
NP_077742.2:n.*685G>T
|
|
NM_024426.4:c.*685G>T
|
NP_077744.3:n.*685G>T
|
|
NM_000378.5:c.*685G>T
|
NP_000369.4:n.*685G>T
|
|
NM_024424.4:c.*685G>T
|
NP_077742.3:n.*685G>T
|
|
NM_024426.5:c.*685G>T
|
NP_077744.4:n.*685G>T
|
|
NM_001367854.1:c.*685G>T
|
NP_001354783.1:n.*685G>T
|
|
NR_160306.1:n.2586G>T
|
|
|
NM_000378.6:c.*685G>T
|
NP_000369.4:n.*685G>T
|
|
NM_001198552.2:c.*685G>T
|
NP_001185481.1:n.*685G>T
|
|
NM_024424.5:c.*685G>T
|
NP_077742.3:n.*685G>T
|
|
NM_024426.6:c.*685G>T
MANE Select
|
NP_077744.4:n.*685G>T
|
|