Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001195228.1 | 880 | Intron | NP_001182157.1 | ||
NM_019013.2 | 880 | Intron | NP_061886.2 | ||
XM_011523944.2 | 880 | Missense Mutation | ACT,CCT | T133P | XP_011522246.1 |
XM_017024778.1 | 880 | Missense Mutation | ACT,CCT | T87P | XP_016880267.1 |