Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000789.3 | 477 | Missense Mutation | AAC,AGC | N148S | NP_000780.1 |
NM_001178057.1 | 477 | Intron | NP_001171528.1 | ||
NM_152830.2 | 477 | Intron | NP_690043.1 | ||
XM_006721737.3 | 477 | Intron | XP_006721800.2 |