| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001323608.1 | 432 | Missense Mutation | CTT,GTT | L99V | NP_001310537.1 |
| NM_001323609.1 | 432 | Missense Mutation | CTT,GTT | L99V | NP_001310538.1 |
| NM_001323610.1 | 432 | Missense Mutation | CTT,GTT | L99V | NP_001310539.1 |
| NM_001323611.1 | 432 | Missense Mutation | CTT,GTT | L25V | NP_001310540.1 |
| NM_005611.3 | 432 | Missense Mutation | CTT,GTT | L99V | NP_005602.3 |
| XM_011523253.2 | 432 | Intron | XP_011521555.1 | ||
| XM_017023513.1 | 432 | Intron | XP_016879002.1 |