Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015695.2 | 289 | Missense Mutation | CCC,CTC | P20L | NP_056510.2 |
XM_005249010.2 | 289 | Missense Mutation | CCC,CTC | P20L | XP_005249067.1 |
XM_005249011.3 | 289 | Missense Mutation | CCC,CTC | P20L | XP_005249068.1 |
XM_011514489.1 | 289 | Missense Mutation | CCC,CTC | P20L | XP_011512791.1 |
XM_011514490.1 | 289 | Missense Mutation | CCC,CTC | P20L | XP_011512792.1 |
XM_011514491.1 | 289 | Missense Mutation | CCC,CTC | P20L | XP_011512793.1 |
XM_011514492.1 | 289 | Missense Mutation | CCC,CTC | P20L | XP_011512794.1 |
XM_017010742.1 | 289 | Missense Mutation | CCC,CTC | P20L | XP_016866231.1 |
XM_017010743.1 | 289 | Intron | XP_016866232.1 |