| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_023011.3 | 105 | Missense Mutation | ACG,GCG | T17A | NP_075387.1 |
| NM_080687.2 | 105 | Missense Mutation | ACG,GCG | T17A | NP_542418.1 |
| XM_005266202.4 | 105 | Intron | XP_005266259.1 | ||
| XM_006719991.3 | 105 | Intron | XP_006720054.1 | ||
| XM_011534844.1 | 105 | Intron | XP_011533146.1 | ||
| XM_011534845.2 | 105 | Intron | XP_011533147.1 | ||
| XM_011534846.1 | 105 | Missense Mutation | ACG,GCG | T17A | XP_011533148.1 |
| XM_011534847.2 | 105 | Intron | XP_011533149.1 | ||
| XM_011534848.2 | 105 | Intron | XP_011533150.1 | ||
| XM_017020709.1 | 105 | Intron | XP_016876198.1 | ||
| XM_017020710.1 | 105 | Intron | XP_016876199.1 | ||
| XM_017020711.1 | 105 | Intron | XP_016876200.1 | ||
| XM_017020712.1 | 105 | Missense Mutation | ACG,GCG | T17A | XP_016876201.1 |