| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001284282.1 | 1350 | Intron | NP_001271211.1 | ||
| NM_001284283.1 | 1350 | Intron | NP_001271212.1 | ||
| NM_001284284.1 | 1350 | Intron | NP_001271213.1 | ||
| NM_001321242.1 | 1350 | Intron | NP_001308171.1 | ||
| NM_001321243.1 | 1350 | Intron | NP_001308172.1 | ||
| NM_001321244.1 | 1350 | Intron | NP_001308173.1 | ||
| NM_001321246.1 | 1350 | Intron | NP_001308175.1 | ||
| NM_001321247.1 | 1350 | Intron | NP_001308176.1 | ||
| NM_001321248.1 | 1350 | Intron | NP_001308177.1 | ||
| NM_001321249.1 | 1350 | Intron | NP_001308178.1 | ||
| NM_001321250.1 | 1350 | Intron | NP_001308179.1 | ||
| NM_001321251.1 | 1350 | Intron | NP_001308180.1 | ||
| NM_030796.4 | 1350 | Intron | NP_110423.3 | ||
| XM_011515539.1 | 1350 | Missense Mutation | CCT,TCT | P162S | XP_011513841.1 |
| XM_011515540.2 | 1350 | Missense Mutation | CCT,TCT | P159S | XP_011513842.1 |
| XM_011515541.2 | 1350 | Missense Mutation | CCT,TCT | P153S | XP_011513843.1 |
| XM_011515546.2 | 1350 | Missense Mutation | CCT,TCT | P145S | XP_011513848.1 |