Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032873.4 | 379 | Missense Mutation | CCC,GCC | P7A | NP_116262.2 |
XM_005271712.3 | 379 | Intron | XP_005271769.1 | ||
XM_011543041.2 | 379 | Intron | XP_011541343.1 | ||
XM_011543042.1 | 379 | UTR 5 | XP_011541344.1 |