| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142958.1 | 1392 | Missense Mutation | CAG,CAT | Q434H | NP_001136430.1 |
| NM_152676.2 | 1392 | Missense Mutation | CAG,CAT | Q358H | NP_689889.1 |
| XM_011525856.1 | 1392 | Missense Mutation | CAG,CAT | Q364H | XP_011524158.1 |
| XM_011525858.2 | 1392 | Intron | XP_011524160.1 | ||
| XM_011525859.1 | 1392 | Intron | XP_011524161.1 | ||
| XM_011525860.1 | 1392 | Intron | XP_011524162.1 | ||
| XM_017025603.1 | 1392 | Missense Mutation | CAG,CAT | Q358H | XP_016881092.1 |
| XM_017025604.1 | 1392 | Missense Mutation | CAG,CAT | Q358H | XP_016881093.1 |