ENST00000332351.9:c.1330T>G
|
ENSP00000331327.5:p.Cys444Gly
|
|
ENST00000379077.9:c.*565T>G
|
ENSP00000368368.5:n.*565T>G
|
|
ENST00000379079.8:c.730T>G
|
ENSP00000368370.2:p.Cys244Gly
|
|
ENST00000448076.9:c.1381T>G
|
ENSP00000413452.5:p.Cys461Gly
|
|
ENST00000452863.10:c.1381T>G
MANE Select
|
ENSP00000415516.5:p.Cys461Gly
|
|
ENST00000526685.2:n.835T>G
|
|
|
ENST00000639563.3:c.1330T>G
|
ENSP00000492269.3:p.Cys444Gly
|
|
ENST00000639907.2:n.524T>G
|
|
|
ENST00000640146.2:c.706T>G
|
ENSP00000491984.2:p.Cys236Gly
|
|
ENST00000650745.1:n.1191T>G
|
|
|
ENST00000650861.1:n.1962T>G
|
|
|
ENST00000650986.1:n.44T>G
|
|
|
ENST00000651459.1:c.152T>G
|
|
|
ENST00000651533.1:n.427T>G
|
|
|
ENST00000651668.1:n.318T>G
|
|
|
ENST00000651794.1:n.1224T>G
|
|
|
ENST00000651819.1:n.306T>G
|
|
|
ENST00000652579.1:n.641T>G
|
|
|
ENST00000652724.1:n.571T>G
|
|
|
ENST00000332351.7:c.1366T>G
|
ENSP00000331327.3:p.Cys456Gly
|
|
ENST00000379077.7:c.*565T>G
|
ENSP00000368368.3:n.*565T>G
|
|
ENST00000379079.6:c.730T>G
|
ENSP00000368370.2:p.Cys244Gly
|
|
ENST00000448076.7:c.1366T>G
|
ENSP00000413452.3:p.Cys456Gly
|
|
ENST00000452863.7:c.1315T>G
|
ENSP00000415516.3:p.Cys439Gly
|
|
ENST00000527882.5:c.347T>G
|
|
|
ENST00000530998.5:c.679T>G
|
ENSP00000435307.1:p.Cys227Gly
|
|
NM_000378.4:c.1315T>G
|
NP_000369.3:p.Cys439Gly
|
|
NM_001198551.1:c.730T>G , LRG_525t2:c.730T>G
|
NP_001185480.1:p.Cys244Gly
|
|
NM_001198552.1:c.679T>G
|
NP_001185481.1:p.Cys227Gly
|
|
NM_024424.3:c.1366T>G
|
NP_077742.2:p.Cys456Gly
|
|
NM_024426.4:c.1366T>G
|
NP_077744.3:p.Cys456Gly
|
|
NM_000378.5:c.1330T>G
|
NP_000369.4:p.Cys444Gly
|
|
NM_024424.4:c.1381T>G
|
NP_077742.3:p.Cys461Gly
|
|
NM_024426.5:c.1381T>G
|
NP_077744.4:p.Cys461Gly
|
|
NM_001367854.1:c.193T>G
|
NP_001354783.1:p.Cys65Gly
|
|
NR_160306.1:n.1713T>G
|
|
|
NM_000378.6:c.1330T>G
|
NP_000369.4:p.Cys444Gly
|
|
NM_001198552.2:c.679T>G
|
NP_001185481.1:p.Cys227Gly
|
|
NM_024424.5:c.1381T>G
|
NP_077742.3:p.Cys461Gly
|
|
NM_024426.6:c.1381T>G
MANE Select
|
NP_077744.4:p.Cys461Gly
|
|