| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184734.1 | 1392 | Intron | NP_001171663.1 | ||
| NM_001184735.1 | 1392 | Intron | NP_001171664.1 | ||
| NM_014010.4 | 1392 | Missense Mutation | AGG,GGG | R1283G | NP_054729.3 |
| NM_198186.3 | 1392 | Missense Mutation | AGG,GGG | R435G | NP_937829.3 |
| NM_198187.3 | 1392 | Missense Mutation | AGG,GGG | R386G | NP_937830.3 |
| NM_198188.2 | 1392 | Intron | NP_937831.1 |