Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001031720.3 | 484 | Missense Mutation | AGC,TGC | S136C | NP_001026890.2 |
NM_024751.3 | 484 | Intron | NP_079027.2 | ||
XM_005263222.3 | 484 | Missense Mutation | AGC,TGC | S136C | XP_005263279.1 |
XM_011532248.2 | 484 | Missense Mutation | AGC,TGC | S136C | XP_011530550.1 |
XM_011532249.2 | 484 | Missense Mutation | AGC,TGC | S136C | XP_011530551.1 |
XM_011532252.2 | 484 | Missense Mutation | AGC,TGC | S136C | XP_011530554.1 |