Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016622.3 | 113 | Missense Mutation | CCC,TCC | P19S | NP_057706.2 |
NM_145644.2 | 113 | Missense Mutation | CCC,TCC | P19S | NP_663619.1 |
XM_005264361.2 | 113 | Intron | XP_005264418.1 |