Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001098416.3 | 3068 | Missense Mutation | CAC,CTC | H954L | NP_001091886.1 |
NM_001308090.1 | 3068 | Missense Mutation | CAC,CTC | H974L | NP_001295019.1 |
NM_015401.4 | 3068 | Missense Mutation | CAC,CTC | H991L | NP_056216.2 |
XM_011538478.1 | 3068 | Missense Mutation | CAC,CTC | H1035L | XP_011536780.1 |
XM_011538479.1 | 3068 | Missense Mutation | CAC,CTC | H998L | XP_011536781.1 |
XM_011538480.1 | 3068 | Missense Mutation | CAC,CTC | H998L | XP_011536782.1 |
XM_011538481.1 | 3068 | Missense Mutation | CAC,CTC | H952L | XP_011536783.1 |
XM_011538482.1 | 3068 | Missense Mutation | CAC,CTC | H952L | XP_011536784.1 |
XM_011538483.1 | 3068 | Intron | XP_011536785.1 | ||
XM_017019455.1 | 3068 | Missense Mutation | CAC,CTC | H1018L | XP_016874944.1 |
XM_017019456.1 | 3068 | Intron | XP_016874945.1 |