| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_005810.3 | 4319 | Intron | NP_005801.3 | ||
| XM_017018682.1 | 4319 | Intron | XP_016874171.1 | ||
| XM_017018683.1 | 4319 | Intron | XP_016874172.1 | ||
| XM_017018684.1 | 4319 | Intron | XP_016874173.1 | ||
| XM_017018685.1 | 4319 | Intron | XP_016874174.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002864.2 | 4319 | Missense Mutation | ACG,GCG | T1432A | NP_002855.2 |
| XM_011520804.2 | 4319 | Missense Mutation | ACG,GCG | T1432A | XP_011519106.1 |
| XM_011520805.2 | 4319 | Missense Mutation | ACG,GCG | T1431A | XP_011519107.1 |
| XM_011520806.1 | 4319 | Intron | XP_011519108.1 | ||
| XM_011520807.2 | 4319 | Intron | XP_011519109.1 | ||
| XM_017019763.1 | 4319 | Missense Mutation | ACG,GCG | T1432A | XP_016875252.1 |
| XM_017019764.1 | 4319 | Missense Mutation | ACG,GCG | T1432A | XP_016875253.1 |
| XM_017019765.1 | 4319 | Missense Mutation | ACG,GCG | T1349A | XP_016875254.1 |
| XM_017019766.1 | 4319 | Missense Mutation | ACG,GCG | T1218A | XP_016875255.1 |
| XM_017019767.1 | 4319 | Intron | XP_016875256.1 |