| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039780.3 | 1062 | Silent Mutation | CCC,CCT | P321P | NP_001034869.1 |
| NM_001287252.1 | 1062 | Silent Mutation | CCC,CCT | P337P | NP_001274181.1 |
| NM_001287253.1 | 1062 | Silent Mutation | CCC,CCT | P322P | NP_001274182.1 |
| XM_017009725.1 | 1062 | Intron | XP_016865214.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098811.1 | 1062 | Silent Mutation | CCA,CCG | P438P | NP_001092281.1 |
| NM_001098812.1 | 1062 | Intron | NP_001092282.1 | ||
| NM_001098813.1 | 1062 | Intron | NP_001092283.1 | ||
| NM_001300798.1 | 1062 | Intron | NP_001287727.1 | ||
| NM_001300799.1 | 1062 | Intron | NP_001287728.1 | ||
| NM_015146.1 | 1062 | Intron | NP_055961.1 | ||
| XM_005271927.2 | 1062 | Silent Mutation | CCA,CCG | P437P | XP_005271984.1 |
| XM_005271928.2 | 1062 | Silent Mutation | CCA,CCG | P436P | XP_005271985.1 |
| XM_005271931.3 | 1062 | Silent Mutation | CCA,CCG | P378P | XP_005271988.1 |
| XM_011543288.1 | 1062 | Silent Mutation | CCA,CCG | P378P | XP_011541590.1 |
| XM_017009254.1 | 1062 | Silent Mutation | CCA,CCG | P435P | XP_016864743.1 |
| XM_017009255.1 | 1062 | Silent Mutation | CCA,CCG | P377P | XP_016864744.1 |
| XM_017009256.1 | 1062 | Silent Mutation | CCA,CCG | P376P | XP_016864745.1 |
| XM_017009257.1 | 1062 | Silent Mutation | CCA,CCG | P376P | XP_016864746.1 |
| XM_017009258.1 | 1062 | Intron | XP_016864747.1 | ||
| XM_017009259.1 | 1062 | Intron | XP_016864748.1 | ||
| XM_017009260.1 | 1062 | Intron | XP_016864749.1 | ||
| XM_017009261.1 | 1062 | Intron | XP_016864750.1 |