|
ENST00000332351.9:c.1001C>T
|
ENSP00000331327.5:p.Thr334Met
|
|
|
ENST00000379077.9:c.*236C>T
|
ENSP00000368368.5:n.*236C>T
|
|
|
ENST00000379079.8:c.401C>T
|
ENSP00000368370.2:p.Thr134Met
|
|
|
ENST00000448076.9:c.1052C>T
|
ENSP00000413452.5:p.Thr351Met
|
|
|
ENST00000452863.10:c.1052C>T
MANE Select
|
ENSP00000415516.5:p.Thr351Met
|
|
|
ENST00000526685.2:n.506C>T
|
|
|
|
ENST00000639563.3:c.1001C>T
|
ENSP00000492269.3:p.Thr334Met
|
|
|
ENST00000639907.2:n.195C>T
|
|
|
|
ENST00000640146.2:c.377C>T
|
ENSP00000491984.2:p.Thr126Met
|
|
|
ENST00000651794.1:n.795C>T
|
|
|
|
ENST00000652579.1:n.212C>T
|
|
|
|
ENST00000652724.1:n.242C>T
|
|
|
|
ENST00000332351.7:c.1037C>T
|
ENSP00000331327.3:p.Thr346Met
|
|
|
ENST00000379077.7:c.*236C>T
|
ENSP00000368368.3:n.*236C>T
|
|
|
ENST00000379079.6:c.401C>T
|
ENSP00000368370.2:p.Thr134Met
|
|
|
ENST00000448076.7:c.1037C>T
|
ENSP00000413452.3:p.Thr346Met
|
|
|
ENST00000452863.7:c.986C>T
|
ENSP00000415516.3:p.Thr329Met
|
|
|
ENST00000526685.1:c.-137C>T
|
ENSP00000436292.1:n.-137C>T
|
|
|
ENST00000527775.1:c.290C>T
|
ENSP00000435351.1:p.Thr97Met
|
|
|
ENST00000527882.5:c.108C>T
|
|
|
|
ENST00000530998.5:c.350C>T
|
ENSP00000435307.1:p.Thr117Met
|
|
|
NM_000378.4:c.986C>T
|
NP_000369.3:p.Thr329Met
|
|
|
NM_001198551.1:c.401C>T , LRG_525t2:c.401C>T
|
NP_001185480.1:p.Thr134Met
|
|
|
NM_001198552.1:c.350C>T
|
NP_001185481.1:p.Thr117Met
|
|
|
NM_024424.3:c.1037C>T
|
NP_077742.2:p.Thr346Met
|
|
|
NM_024426.4:c.1037C>T
|
NP_077744.3:p.Thr346Met
|
|
|
NM_000378.5:c.1001C>T
|
NP_000369.4:p.Thr334Met
|
|
|
NM_024424.4:c.1052C>T
|
NP_077742.3:p.Thr351Met
|
|
|
NM_024426.5:c.1052C>T
|
NP_077744.4:p.Thr351Met
|
|
|
NM_001367854.1:c.-137C>T
|
NP_001354783.1:n.-137C>T
|
|
|
NR_160306.1:n.1384C>T
|
|
|
|
NM_000378.6:c.1001C>T
|
NP_000369.4:p.Thr334Met
|
|
|
NM_001198552.2:c.350C>T
|
NP_001185481.1:p.Thr117Met
|
|
|
NM_024424.5:c.1052C>T
|
NP_077742.3:p.Thr351Met
|
|
|
NM_024426.6:c.1052C>T
MANE Select
|
NP_077744.4:p.Thr351Met
|
|
