| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014966.3 | 455 | UTR 5 | NP_055781.2 | ||
| NM_138615.2 | 455 | Missense Mutation | GAT,GGT | D10G | NP_619520.1 |
| XM_006713033.1 | 455 | Intron | XP_006713096.1 | ||
| XM_011533490.1 | 455 | UTR 5 | XP_011531792.1 | ||
| XM_011533491.1 | 455 | UTR 5 | XP_011531793.1 | ||
| XM_011533492.2 | 455 | UTR 5 | XP_011531794.1 | ||
| XM_011533493.1 | 455 | UTR 5 | XP_011531795.1 | ||
| XM_011533494.2 | 455 | Missense Mutation | GAT,GGT | D10G | XP_011531796.1 |
| XM_011533495.1 | 455 | Missense Mutation | GAT,GGT | D10G | XP_011531797.1 |
| XM_011533496.1 | 455 | UTR 5 | XP_011531798.1 | ||
| XM_011533497.2 | 455 | UTR 5 | XP_011531799.1 | ||
| XM_011533498.1 | 455 | UTR 5 | XP_011531800.1 | ||
| XM_017005914.1 | 455 | Silent Mutation | AGA,AGG | R44R | XP_016861403.1 |
| XM_017005915.1 | 455 | Intron | XP_016861404.1 | ||
| XM_017005916.1 | 455 | Missense Mutation | GAT,GGT | D10G | XP_016861405.1 |
| XM_017005917.1 | 455 | UTR 5 | XP_016861406.1 |