Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001136264.1 | 497 | Missense Mutation | GCT,TCT | A115S | NP_001129736.1 |
NM_001136266.1 | 497 | Missense Mutation | TGC,TTC | C111F | NP_001129738.1 |
NM_001136267.1 | 497 | Missense Mutation | GCT,TCT | A105S | NP_001129739.1 |
NM_001136268.1 | 497 | Missense Mutation | GCT,TCT | A55S | NP_001129740.1 |
NM_001136269.1 | 497 | Intron | NP_001129741.1 | ||
NM_014764.3 | 497 | Missense Mutation | GCT,TCT | A137S | NP_055579.1 |