| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_138701.3 | 134 | Missense Mutation | CGT,GGT | R17G | NP_619646.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193311.1 | 134 | Intron | NP_001180240.1 | ||
| NM_001193312.1 | 134 | Intron | NP_001180241.1 | ||
| NM_001193313.1 | 134 | Intron | NP_001180242.1 | ||
| NM_024728.2 | 134 | Intron | NP_079004.1 | ||
| XM_006715775.3 | 134 | Intron | XP_006715838.1 | ||
| XM_011515525.2 | 134 | Intron | XP_011513827.1 | ||
| XM_011515526.2 | 134 | Intron | XP_011513828.1 | ||
| XM_011515527.2 | 134 | Intron | XP_011513829.1 | ||
| XM_011515528.2 | 134 | Intron | XP_011513830.1 | ||
| XM_011515529.2 | 134 | Intron | XP_011513831.1 | ||
| XM_011515530.2 | 134 | Intron | XP_011513832.1 | ||
| XM_017012621.1 | 134 | Intron | XP_016868110.1 | ||
| XM_017012622.1 | 134 | Intron | XP_016868111.1 |