| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142603.2 | 291 | Missense Mutation | CCT,CTT | P45L | NP_001136075.1 |
| NM_014773.4 | 291 | Missense Mutation | CCT,CTT | P45L | NP_055588.3 |
| XM_005268547.3 | 291 | Missense Mutation | CCT,CTT | P45L | XP_005268604.1 |
| XM_005268548.3 | 291 | Missense Mutation | CCT,CTT | P45L | XP_005268605.1 |
| XM_005268552.2 | 291 | Missense Mutation | CCT,CTT | P45L | XP_005268609.1 |
| XM_006714812.3 | 291 | Intron | XP_006714875.1 | ||
| XM_011537715.1 | 291 | Missense Mutation | CCT,CTT | P45L | XP_011536017.1 |
| XM_011537716.2 | 291 | Missense Mutation | CCT,CTT | P45L | XP_011536018.1 |