Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001256799.2 | 489 | Missense Mutation | AAT,AGT | N28S | NP_001243728.1 |
NM_001289745.1 | 489 | Missense Mutation | NP_001276674.1 | ||
NM_001289746.1 | 489 | Intron | NP_001276675.1 | ||
NM_002046.5 | 489 | Missense Mutation | NP_002037.2 |