Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001276700.1 | 1010 | Missense Mutation | CCC,GCC | P269A | NP_001263629.1 |
NM_138329.2 | 1010 | Missense Mutation | CCC,GCC | P269A | NP_612202.2 |
XM_011519931.1 | 1010 | Missense Mutation | CCC,GCC | P269A | XP_011518233.1 |
XM_017017252.1 | 1010 | Missense Mutation | CCC,GCC | P269A | XP_016872741.1 |
XM_017017253.1 | 1010 | Missense Mutation | CCC,GCC | P107A | XP_016872742.1 |