Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145166.1 | 343 | Intron | NP_001138638.1 | ||
NM_001145167.1 | 343 | Intron | NP_001138639.1 | ||
NM_005788.3 | 343 | Silent Mutation | CCA,CCC | P42P | NP_005779.1 |
XM_011519836.2 | 343 | Intron | XP_011518138.1 | ||
XM_017017081.1 | 343 | Missense Mutation | CAC,CCC | H26P | XP_016872570.1 |