| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_021003.4 | 116 | Intron | NP_066283.1 | ||
| NM_177951.2 | 116 | Intron | NP_808820.1 | ||
| NM_177952.2 | 116 | Missense Mutation | CTA,GTA | L9V | NP_808821.2 |
| XM_005267779.1 | 116 | UTR 5 | XP_005267836.1 | ||
| XM_005267781.1 | 116 | Intron | XP_005267838.1 | ||
| XM_011536872.1 | 116 | Intron | XP_011535174.1 | ||
| XM_011536876.1 | 116 | Intron | XP_011535178.1 | ||
| XM_011536877.1 | 116 | Intron | XP_011535179.1 | ||
| XM_011536878.1 | 116 | Intron | XP_011535180.1 | ||
| XM_011536879.2 | 116 | Intron | XP_011535181.1 | ||
| XM_011536880.2 | 116 | Intron | XP_011535182.1 | ||
| XM_011536881.2 | 116 | Intron | XP_011535183.1 | ||
| XM_011536882.2 | 116 | Intron | XP_011535184.1 | ||
| XM_011536883.1 | 116 | Intron | XP_011535185.1 | ||
| XM_011536884.1 | 116 | Intron | XP_011535186.1 | ||
| XM_017021381.1 | 116 | Intron | XP_016876870.1 | ||
| XM_017021382.1 | 116 | Intron | XP_016876871.1 | ||
| XM_017021383.1 | 116 | Intron | XP_016876872.1 | ||
| XM_017021384.1 | 116 | Intron | XP_016876873.1 | ||
| XM_017021385.1 | 116 | Intron | XP_016876874.1 | ||
| XM_017021386.1 | 116 | Intron | XP_016876875.1 | ||
| XM_017021387.1 | 116 | Intron | XP_016876876.1 |