| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001007271.1 | 468 | Missense Mutation | ACG,ATG | T138M | NP_001007272.1 |
| NM_001007272.1 | 468 | Intron | NP_001007273.1 | ||
| NM_001007273.1 | 468 | Intron | NP_001007274.1 | ||
| NM_001320842.1 | 468 | Intron | NP_001307771.1 | ||
| NM_001320843.1 | 468 | Intron | NP_001307772.1 | ||
| NM_016364.3 | 468 | Intron | NP_057448.3 | ||
| XM_005269883.3 | 468 | Silent Mutation | CAC,CAT | H65H | XP_005269940.1 |
| XM_005269884.4 | 468 | Intron | XP_005269941.3 | ||
| XM_005269887.1 | 468 | Intron | XP_005269944.1 | ||
| XM_005269890.1 | 468 | Intron | XP_005269947.1 | ||
| XM_011539853.1 | 468 | UTR 5 | XP_011538155.1 | ||
| XM_011539854.2 | 468 | Intron | XP_011538156.1 | ||
| XM_011539855.1 | 468 | Intron | XP_011538157.1 | ||
| XM_011539856.2 | 468 | Intron | XP_011538158.1 | ||
| XM_017016313.1 | 468 | Intron | XP_016871802.1 | ||
| XM_017016314.1 | 468 | Silent Mutation | CAC,CAT | H65H | XP_016871803.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001174156.1 | 468 | Intron | NP_001167627.1 | ||
| NM_144660.2 | 468 | Intron | NP_653261.1 | ||
| XM_005269541.4 | 468 | Intron | XP_005269598.1 | ||
| XM_011539311.1 | 468 | Intron | XP_011537613.1 | ||
| XM_011539312.2 | 468 | Intron | XP_011537614.1 | ||
| XM_017015738.1 | 468 | Intron | XP_016871227.1 | ||
| XM_017015739.1 | 468 | Intron | XP_016871228.1 |