| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243313.1 | 312 | Missense Mutation | CCA,CTA | P122L | NP_001230242.1 |
| NM_015690.4 | 312 | Missense Mutation | CCA,CTA | P122L | NP_056505.2 |
| XM_005246464.1 | 312 | Missense Mutation | CCA,CTA | P122L | XP_005246521.1 |
| XM_011510959.1 | 312 | Missense Mutation | CCA,CTA | P122L | XP_011509261.1 |
| XM_011510960.1 | 312 | Missense Mutation | CCA,CTA | P68L | XP_011509262.1 |
| XM_011510961.1 | 312 | Intron | XP_011509263.1 | ||
| XM_017003804.1 | 312 | Missense Mutation | CCA,CTA | P122L | XP_016859293.1 |
| XM_017003805.1 | 312 | UTR 5 | XP_016859294.1 |