| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003635.3 | 3225 | Missense Mutation | CTT,GTT | L820V | NP_003626.1 |
| XM_005270255.3 | 3225 | Missense Mutation | GAC,GAG | D807E | XP_005270312.1 |
| XM_005270256.3 | 3225 | Missense Mutation | CTT,GTT | L446V | XP_005270313.1 |
| XM_011540310.2 | 3225 | Missense Mutation | CTT,GTT | L820V | XP_011538612.1 |
| XM_017016857.1 | 3225 | Missense Mutation | CTT,GTT | L343V | XP_016872346.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001242487.1 | 3225 | Intron | NP_001229416.1 | ||
| NM_001242488.1 | 3225 | Intron | NP_001229417.1 | ||
| NM_015037.3 | 3225 | Intron | NP_055852.2 | ||
| XM_005269648.2 | 3225 | Intron | XP_005269705.1 | ||
| XM_005269653.3 | 3225 | Intron | XP_005269710.1 | ||
| XM_005269655.3 | 3225 | Intron | XP_005269712.1 | ||
| XM_006717725.3 | 3225 | Intron | XP_006717788.1 | ||
| XM_011539544.1 | 3225 | Intron | XP_011537846.1 | ||
| XM_017015978.1 | 3225 | Intron | XP_016871467.1 |