| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152543.2 | 3402 | Intron | NP_689756.2 | ||
| XM_011531671.2 | 3402 | Intron | XP_011529973.1 | ||
| XM_011531672.2 | 3402 | Intron | XP_011529974.1 | ||
| XM_017007808.1 | 3402 | Intron | XP_016863297.1 | ||
| XM_017007809.1 | 3402 | Intron | XP_016863298.1 | ||
| XM_017007810.1 | 3402 | Intron | XP_016863299.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001323916.1 | 3402 | Missense Mutation | ATG,GTG | M1085V | NP_001310845.1 |
| NM_020840.2 | 3402 | Missense Mutation | ATG,GTG | M1062V | NP_065891.1 |
| XM_005263156.1 | 3402 | Missense Mutation | ATG,GTG | M1115V | XP_005263213.1 |
| XM_005263158.1 | 3402 | Missense Mutation | ATG,GTG | M1092V | XP_005263215.1 |
| XM_005263160.3 | 3402 | Intron | XP_005263217.1 | ||
| XM_011532154.2 | 3402 | Missense Mutation | ATG,GTG | M1060V | XP_011530456.1 |
| XM_017008487.1 | 3402 | Missense Mutation | ATG,GTG | M1098V | XP_016863976.1 |