ENST00000332351.9:c.*741G>T
|
ENSP00000331327.5:n.*741G>T
|
|
ENST00000379077.9:c.*1494G>T
|
ENSP00000368368.5:n.*1494G>T
|
|
ENST00000379079.8:c.*741G>T
|
ENSP00000368370.2:n.*741G>T
|
|
ENST00000452863.10:c.*741G>T
MANE Select
|
ENSP00000415516.5:n.*741G>T
|
|
ENST00000639907.2:n.1444G>T
|
|
|
ENST00000640146.2:c.*741G>T
|
ENSP00000491984.2:n.*741G>T
|
|
ENST00000650745.1:n.2120G>T
|
|
|
ENST00000650861.1:n.2882G>T
|
|
|
ENST00000651459.1:c.1081G>T
|
|
|
ENST00000651533.1:n.1347G>T
|
|
|
ENST00000651668.1:n.1247G>T
|
|
|
ENST00000651794.1:n.2153G>T
|
|
|
ENST00000651819.1:n.1235G>T
|
|
|
ENST00000652579.1:n.1570G>T
|
|
|
ENST00000652724.1:n.1500G>T
|
|
|
ENST00000332351.7:c.*741G>T
|
ENSP00000331327.3:n.*741G>T
|
|
ENST00000379077.7:c.*1494G>T
|
ENSP00000368368.3:n.*1494G>T
|
|
ENST00000379079.6:c.*741G>T
|
ENSP00000368370.2:n.*741G>T
|
|
ENST00000452863.7:c.2235G>T
|
ENSP00000415516.3:n.2235G>T
|
|
ENST00000530998.5:c.*741G>T
|
ENSP00000435307.1:n.*741G>T
|
|
NM_000378.4:c.*741G>T
|
NP_000369.3:n.*741G>T
|
|
NM_001198551.1:c.*741G>T , LRG_525t2:c.*741G>T
|
NP_001185480.1:n.*741G>T
|
|
NM_001198552.1:c.*741G>T
|
NP_001185481.1:n.*741G>T
|
|
NM_024424.3:c.*741G>T
|
NP_077742.2:n.*741G>T
|
|
NM_024426.4:c.*741G>T
|
NP_077744.3:n.*741G>T
|
|
NM_000378.5:c.*741G>T
|
NP_000369.4:n.*741G>T
|
|
NM_024424.4:c.*741G>T
|
NP_077742.3:n.*741G>T
|
|
NM_024426.5:c.*741G>T
|
NP_077744.4:n.*741G>T
|
|
NM_001367854.1:c.*741G>T
|
NP_001354783.1:n.*741G>T
|
|
NR_160306.1:n.2642G>T
|
|
|
NM_000378.6:c.*741G>T
|
NP_000369.4:n.*741G>T
|
|
NM_001198552.2:c.*741G>T
|
NP_001185481.1:n.*741G>T
|
|
NM_024424.5:c.*741G>T
|
NP_077742.3:n.*741G>T
|
|
NM_024426.6:c.*741G>T
MANE Select
|
NP_077744.4:n.*741G>T
|
|