ENST00000332351.9:c.984_985delinsAT
|
ENSP00000331327.5:p.Ser329Cys
|
|
ENST00000379077.9:c.*219_*220delinsAT
|
ENSP00000368368.5:n.*219_*220delinsAT
|
|
ENST00000379079.8:c.384_385delinsAT
|
ENSP00000368370.2:p.Ser129Cys
|
|
ENST00000448076.9:c.1035_1036delinsAT
|
ENSP00000413452.5:p.Ser346Cys
|
|
ENST00000452863.10:c.1035_1036delinsAT
MANE Select
|
ENSP00000415516.5:p.Ser346Cys
|
|
ENST00000526685.2:n.489_490delinsAT
|
|
|
ENST00000639563.3:c.984_985delinsAT
|
ENSP00000492269.3:p.Ser329Cys
|
|
ENST00000639907.2:n.178_179delinsAT
|
|
|
ENST00000640146.2:c.360_361delinsAT
|
ENSP00000491984.2:p.Ser121Cys
|
|
ENST00000651794.1:n.778_779delinsAT
|
|
|
ENST00000652579.1:n.195_196delinsAT
|
|
|
ENST00000652724.1:n.225_226delinsAT
|
|
|
ENST00000332351.7:c.1020_1021delinsAT
|
ENSP00000331327.3:p.Ser341Cys
|
|
ENST00000379077.7:c.*219_*220delinsAT
|
ENSP00000368368.3:n.*219_*220delinsAT
|
|
ENST00000379079.6:c.384_385delinsAT
|
ENSP00000368370.2:p.Ser129Cys
|
|
ENST00000448076.7:c.1020_1021delinsAT
|
ENSP00000413452.3:p.Ser341Cys
|
|
ENST00000452863.7:c.969_970delinsAT
|
ENSP00000415516.3:p.Ser324Cys
|
|
ENST00000526685.1:c.-154_-153delinsAT
|
ENSP00000436292.1:n.-154_-153delinsAT
|
|
ENST00000527775.1:c.273_274delinsAT
|
ENSP00000435351.1:p.Ser92Cys
|
|
ENST00000527882.5:c.91_92delinsAT
|
|
|
ENST00000530998.5:c.333_334delinsAT
|
ENSP00000435307.1:p.Ser112Cys
|
|
NM_000378.4:c.969_970delinsAT
|
NP_000369.3:p.Ser324Cys
|
|
NM_001198551.1:c.384_385delinsAT , LRG_525t2:c.384_385delinsAT
|
NP_001185480.1:p.Ser129Cys
|
|
NM_001198552.1:c.333_334delinsAT
|
NP_001185481.1:p.Ser112Cys
|
|
NM_024424.3:c.1020_1021delinsAT
|
NP_077742.2:p.Ser341Cys
|
|
NM_024426.4:c.1020_1021delinsAT
|
NP_077744.3:p.Ser341Cys
|
|
NM_000378.5:c.984_985delinsAT
|
NP_000369.4:p.Ser329Cys
|
|
NM_024424.4:c.1035_1036delinsAT
|
NP_077742.3:p.Ser346Cys
|
|
NM_024426.5:c.1035_1036delinsAT
|
NP_077744.4:p.Ser346Cys
|
|
NM_001367854.1:c.-154_-153delinsAT
|
NP_001354783.1:n.-154_-153delinsAT
|
|
NR_160306.1:n.1367_1368delinsAT
|
|
|
NM_000378.6:c.984_985delinsAT
|
NP_000369.4:p.Ser329Cys
|
|
NM_001198552.2:c.333_334delinsAT
|
NP_001185481.1:p.Ser112Cys
|
|
NM_024424.5:c.1035_1036delinsAT
|
NP_077742.3:p.Ser346Cys
|
|
NM_024426.6:c.1035_1036delinsAT
MANE Select
|
NP_077744.4:p.Ser346Cys
|
|