ENST00000330062.8:c.645_646insCGCAACC
MANE Select
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ENSP00000331897.4:p.Gly216ArgfsTer?
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ENST00000330062.7:c.645_646insCGCAACC
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ENSP00000331897.3:p.Gly216ArgfsTer?
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ENST00000540499.2:c.489_490insCGCAACC
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ENSP00000446147.2:p.Gly164ArgfsTer?
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ENST00000559482.5:c.318_319insCGCAACC
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ENSP00000453016.1:p.Gly107ArgfsTer?
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ENST00000560061.1:c.*270_*271insCGCAACC
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ENSP00000453254.1:n.*270_*271insCGCAACC
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NM_001289910.1:c.489_490insCGCAACC , LRG_611t1:c.489_490insCGCAACC
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NP_001276839.1:p.Gly164ArgfsTer?
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NM_001290114.1:c.255_256insCGCAACC
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NP_001277043.1:p.Gly86ArgfsTer?
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NM_002168.3:c.645_646insCGCAACC , LRG_611t2:c.645_646insCGCAACC
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NP_002159.2:p.Gly216ArgfsTer?
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NM_001290114.2:c.255_256insCGCAACC
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NP_001277043.1:p.Gly86ArgfsTer?
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NM_002168.4:c.645_646insCGCAACC
MANE Select
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NP_002159.2:p.Gly216ArgfsTer?
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