Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001134473.2 | 2138 | Intron | NP_001127945.1 | ||
NM_001278184.1 | 2138 | Intron | NP_001265113.1 | ||
NM_014615.3 | 2138 | Intron | NP_055430.1 | ||
XM_005255859.4 | 2138 | Silent Mutation | CTA,TTA | L598L | XP_005255916.3 |
XM_005255860.3 | 2138 | Silent Mutation | CTA,TTA | L598L | XP_005255917.3 |
XM_005255861.4 | 2138 | Silent Mutation | CTA,TTA | L598L | XP_005255918.3 |
XM_005255863.4 | 2138 | Intron | XP_005255920.1 | ||
XM_005255864.4 | 2138 | Intron | XP_005255921.1 | ||
XM_005255865.4 | 2138 | Intron | XP_005255922.1 | ||
XM_011522965.2 | 2138 | Intron | XP_011521267.1 | ||
XM_011522966.2 | 2138 | Intron | XP_011521268.1 | ||
XM_017023083.1 | 2138 | Intron | XP_016878572.1 | ||
XM_017023084.1 | 2138 | Silent Mutation | CTA,TTA | L709L | XP_016878573.1 |