|
ENST00000332351.9:c.1102_1103insAG
|
ENSP00000331327.5:p.Arg368GlnfsTer?
|
|
|
ENST00000379077.9:c.*337_*338insAG
|
ENSP00000368368.5:n.*337_*338insAG
|
|
|
ENST00000379079.8:c.502_503insAG
|
ENSP00000368370.2:p.Arg168GlnfsTer?
|
|
|
ENST00000448076.9:c.1153_1154insAG
|
ENSP00000413452.5:p.Arg385GlnfsTer?
|
|
|
ENST00000452863.10:c.1153_1154insAG
MANE Select
|
ENSP00000415516.5:p.Arg385GlnfsTer?
|
|
|
ENST00000526685.2:n.607_608insAG
|
|
|
|
ENST00000639563.3:c.1102_1103insAG
|
ENSP00000492269.3:p.Arg368GlnfsTer?
|
|
|
ENST00000639907.2:n.296_297insAG
|
|
|
|
ENST00000640146.2:c.478_479insAG
|
ENSP00000491984.2:p.Arg160GlnfsTer?
|
|
|
ENST00000650861.1:n.1734_1735insAG
|
|
|
|
ENST00000651459.1:c.35+3580_35+3581insAG
|
|
|
|
ENST00000651668.1:n.90_91insAG
|
|
|
|
ENST00000651794.1:n.896_897insAG
|
|
|
|
ENST00000651819.1:n.78_79insAG
|
|
|
|
ENST00000652579.1:n.313_314insAG
|
|
|
|
ENST00000652724.1:n.343_344insAG
|
|
|
|
ENST00000332351.7:c.1138_1139insAG
|
ENSP00000331327.3:p.Arg380GlnfsTer?
|
|
|
ENST00000379077.7:c.*337_*338insAG
|
ENSP00000368368.3:n.*337_*338insAG
|
|
|
ENST00000379079.6:c.502_503insAG
|
ENSP00000368370.2:p.Arg168GlnfsTer?
|
|
|
ENST00000448076.7:c.1138_1139insAG
|
ENSP00000413452.3:p.Arg380GlnfsTer?
|
|
|
ENST00000452863.7:c.1087_1088insAG
|
ENSP00000415516.3:p.Arg363GlnfsTer?
|
|
|
ENST00000526685.1:c.-36_-35insAG
|
ENSP00000436292.1:n.-36_-35insAG
|
|
|
ENST00000527775.1:c.391_392insAG
|
ENSP00000435351.1:p.Arg131GlnfsTer?
|
|
|
ENST00000527882.5:c.209_210insAG
|
|
|
|
ENST00000530998.5:c.451_452insAG
|
ENSP00000435307.1:p.Arg151GlnfsTer?
|
|
|
NM_000378.4:c.1087_1088insAG
|
NP_000369.3:p.Arg363GlnfsTer?
|
|
|
NM_001198551.1:c.502_503insAG , LRG_525t2:c.502_503insAG
|
NP_001185480.1:p.Arg168GlnfsTer?
|
|
|
NM_001198552.1:c.451_452insAG
|
NP_001185481.1:p.Arg151GlnfsTer?
|
|
|
NM_024424.3:c.1138_1139insAG
|
NP_077742.2:p.Arg380GlnfsTer?
|
|
|
NM_024426.4:c.1138_1139insAG
|
NP_077744.3:p.Arg380GlnfsTer?
|
|
|
NM_000378.5:c.1102_1103insAG
|
NP_000369.4:p.Arg368GlnfsTer?
|
|
|
NM_024424.4:c.1153_1154insAG
|
NP_077742.3:p.Arg385GlnfsTer?
|
|
|
NM_024426.5:c.1153_1154insAG
|
NP_077744.4:p.Arg385GlnfsTer?
|
|
|
NM_001367854.1:c.-36_-35insAG
|
NP_001354783.1:n.-36_-35insAG
|
|
|
NR_160306.1:n.1485_1486insAG
|
|
|
|
NM_000378.6:c.1102_1103insAG
|
NP_000369.4:p.Arg368GlnfsTer?
|
|
|
NM_001198552.2:c.451_452insAG
|
NP_001185481.1:p.Arg151GlnfsTer?
|
|
|
NM_024424.5:c.1153_1154insAG
|
NP_077742.3:p.Arg385GlnfsTer?
|
|
|
NM_024426.6:c.1153_1154insAG
MANE Select
|
NP_077744.4:p.Arg385GlnfsTer?
|
|
