| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004308.3 | 195 | Intron | NP_004299.1 | ||
| XM_011520095.1 | 195 | Intron | XP_011518397.1 | ||
| XM_017017720.1 | 195 | Intron | XP_016873209.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184751.1 | 195 | Missense Mutation | CTC,GTC | L59V | NP_001171680.1 |
| NM_024741.2 | 195 | Missense Mutation | CTC,GTC | L67V | NP_079017.1 |