| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286638.1 | 354 | Intron | NP_001273567.1 | ||
| NM_153251.3 | 354 | Intron | NP_694983.2 | ||
| XM_006719795.1 | 354 | Missense Mutation | CAC,CGC | H246R | XP_006719858.1 |
| XM_006719796.1 | 354 | Missense Mutation | CAC,CGC | H246R | XP_006719859.1 |
| XM_006719797.1 | 354 | Missense Mutation | CAC,CGC | H246R | XP_006719860.1 |
| XM_011535030.2 | 354 | Missense Mutation | CAC,CGC | H98R | XP_011533332.1 |
| XM_017020525.1 | 354 | Intron | XP_016876014.1 | ||
| XM_017020526.1 | 354 | Missense Mutation | CAC,CGC | H167R | XP_016876015.1 |
| XM_017020527.1 | 354 | Missense Mutation | CAC,CGC | H167R | XP_016876016.1 |