Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024589.2 | 716 | Intron | NP_078865.1 | ||
XM_006720947.3 | 716 | Missense Mutation | GCC,TCC | A237S | XP_006721010.1 |
XM_006720948.3 | 716 | Missense Mutation | GCC,TCC | A147S | XP_006721011.1 |