| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014591.4 | 560 | Intron | NP_055406.2 | ||
| NM_173191.2 | 560 | Intron | NP_775283.1 | ||
| NM_173192.2 | 560 | Intron | NP_775284.1 | ||
| NM_173193.2 | 560 | Missense Mutation | CTC,TTC | L70F | NP_775285.1 |
| NM_173194.2 | 560 | Intron | NP_775286.1 | ||
| NM_173195.2 | 560 | Intron | NP_775287.1 | ||
| NM_173197.2 | 560 | Intron | NP_775289.1 | ||
| XM_005269729.2 | 560 | Intron | XP_005269786.1 | ||
| XM_005269730.2 | 560 | Intron | XP_005269787.1 | ||
| XM_006717812.2 | 560 | Intron | XP_006717875.1 | ||
| XM_011539731.2 | 560 | Intron | XP_011538033.1 | ||
| XM_017016161.1 | 560 | Intron | XP_016871650.1 |