Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001190328.1 | 38 | Intron | NP_001177257.1 | ||
NM_198537.3 | 38 | Missense Mutation | AGA,GGA | R53G | NP_940939.2 |
XM_005259903.4 | 38 | Missense Mutation | AGA,GGA | R126G | XP_005259960.1 |
XM_011527996.2 | 38 | Missense Mutation | AGA,GGA | R126G | XP_011526298.1 |
XM_011527997.1 | 38 | UTR 5 | XP_011526299.1 | ||
XM_011527998.2 | 38 | Intron | XP_011526300.1 | ||
XM_011527999.1 | 38 | UTR 5 | XP_011526301.1 | ||
XM_017026770.1 | 38 | UTR 5 | XP_016882259.1 | ||
XM_017026771.1 | 38 | UTR 5 | XP_016882260.1 |