Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001031690.2 | 721 | Intron | NP_001026860.2 | ||
NM_001278297.1 | 721 | Intron | NP_001265226.1 | ||
NM_014690.4 | 721 | Intron | NP_055505.3 | ||
XM_005250073.3 | 721 | Intron | XP_005250130.1 | ||
XM_006716186.2 | 721 | Intron | XP_006716249.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001010972.1 | 721 | Missense Mutation | CAT,CTT | H223L | NP_001010972.1 |
NM_003461.4 | 721 | Missense Mutation | CAT,CTT | H223L | NP_003452.1 |
XM_011516569.2 | 721 | Missense Mutation | CAT,CTT | H192L | XP_011514871.2 |
XM_017012587.1 | 721 | Missense Mutation | CAT,CTT | H282L | XP_016868076.1 |