| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001197301.1 | 377 | Intron | NP_001184230.1 | ||
| NM_001197302.1 | 377 | Intron | NP_001184231.1 | ||
| NM_014419.3 | 377 | Missense Mutation | ATC,CTC | I104L | NP_055234.1 |
| XM_006723142.2 | 377 | Missense Mutation | ATC,CTC | I119L | XP_006723205.1 |
| XM_011526724.1 | 377 | Missense Mutation | ATC,CTC | I127L | XP_011525026.1 |
| XM_011526725.1 | 377 | Missense Mutation | ATC,CTC | I111L | XP_011525027.1 |
| XM_011526726.2 | 377 | Missense Mutation | ATC,CTC | I111L | XP_011525028.1 |
| XM_011526727.2 | 377 | Missense Mutation | ATC,CTC | I127L | XP_011525029.1 |
| XM_011526728.2 | 377 | Intron | XP_011525030.1 | ||
| XM_011526729.1 | 377 | Missense Mutation | ATC,CTC | I29L | XP_011525031.1 |
| XM_017026593.1 | 377 | Missense Mutation | ATC,CTC | I29L | XP_016882082.1 |