| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_138424.1 | 2037 | Missense Mutation | CAT,CGT | H513R | NP_612433.1 |
| XM_005251683.4 | 2037 | Missense Mutation | ATT,GTT | I658V | XP_005251740.1 |
| XM_006716947.2 | 2037 | Missense Mutation | ATT,GTT | I624V | XP_006717010.1 |
| XM_011518190.2 | 2037 | Missense Mutation | ATT,GTT | I716V | XP_011516492.1 |
| XM_011518191.2 | 2037 | Missense Mutation | CAT,CGT | H709R | XP_011516493.1 |
| XM_011518192.2 | 2037 | Intron | XP_011516494.1 | ||
| XM_011518193.2 | 2037 | Intron | XP_011516495.1 | ||
| XM_017014240.1 | 2037 | Missense Mutation | ATT,GTT | I393V | XP_016869729.1 |