|
NM_024426.6:c.1408C>T
MANE Select
|
NP_077744.4:p.His470Tyr
|
|
ENST00000452863.10:c.1408C>T
MANE Select
|
ENSP00000415516.5:p.His470Tyr
|
|
NM_000378.4:c.1342C>T
|
NP_000369.3:p.His448Tyr
|
|
NM_000378.5:c.1357C>T
|
NP_000369.4:p.His453Tyr
|
|
NM_000378.6:c.1357C>T
|
NP_000369.4:p.His453Tyr
|
|
NM_001198551.1:c.757C>T , LRG_525t2:c.757C>T
|
NP_001185480.1:p.His253Tyr
|
|
NM_001198552.1:c.706C>T
|
NP_001185481.1:p.His236Tyr
|
|
NM_001198552.2:c.706C>T
|
NP_001185481.1:p.His236Tyr
|
|
NM_001367854.1:c.220C>T
|
NP_001354783.1:p.His74Tyr
|
|
NM_024424.3:c.1393C>T
|
NP_077742.2:p.His465Tyr
|
|
NM_024424.4:c.1408C>T
|
NP_077742.3:p.His470Tyr
|
|
NM_024424.5:c.1408C>T
|
NP_077742.3:p.His470Tyr
|
|
NM_024426.4:c.1393C>T
|
NP_077744.3:p.His465Tyr
|
|
NM_024426.5:c.1408C>T
|
NP_077744.4:p.His470Tyr
|
|
NR_160306.1:n.1740C>T
|
|
|
ENST00000332351.7:c.1393C>T
|
ENSP00000331327.3:p.His465Tyr
|
|
ENST00000332351.9:c.1357C>T
|
ENSP00000331327.5:p.His453Tyr
|
|
ENST00000379077.7:c.*592C>T
|
ENSP00000368368.3:n.*592C>T
|
|
ENST00000379077.9:c.*592C>T
|
ENSP00000368368.5:n.*592C>T
|
|
ENST00000379079.6:c.757C>T
|
ENSP00000368370.2:p.His253Tyr
|
|
ENST00000379079.8:c.757C>T
|
ENSP00000368370.2:p.His253Tyr
|
|
ENST00000448076.7:c.1393C>T
|
ENSP00000413452.3:p.His465Tyr
|
|
ENST00000448076.9:c.1408C>T
|
ENSP00000413452.5:p.His470Tyr
|
|
ENST00000452863.7:c.1342C>T
|
ENSP00000415516.3:p.His448Tyr
|
|
ENST00000526685.2:n.862C>T
|
|
|
ENST00000527882.5:c.374C>T
|
|
|
ENST00000530998.5:c.706C>T
|
ENSP00000435307.1:p.His236Tyr
|
|
ENST00000639563.3:c.1357C>T
|
ENSP00000492269.3:p.His453Tyr
|
|
ENST00000639907.2:n.551C>T
|
|
|
ENST00000640146.2:c.733C>T
|
ENSP00000491984.2:p.His245Tyr
|
|
ENST00000650745.1:n.1218C>T
|
|
|
ENST00000650861.1:n.1989C>T
|
|
|
ENST00000650986.1:n.71C>T
|
|
|
ENST00000651459.1:c.179C>T
|
|
|
ENST00000651533.1:n.454C>T
|
|
|
ENST00000651668.1:n.345C>T
|
|
|
ENST00000651794.1:n.1251C>T
|
|
|
ENST00000651819.1:n.333C>T
|
|
|
ENST00000652579.1:n.668C>T
|
|
|
ENST00000652724.1:n.598C>T
|
|
