ENST00000285021.12:c.1769T>G
MANE Select
|
ENSP00000285021.8:p.Met590Arg
|
|
ENST00000285021.11:c.1769T>G
|
ENSP00000285021.7:p.Met590Arg
|
|
ENST00000476581.6:c.*1222T>G
|
ENSP00000424548.1:n.*1222T>G
|
|
NM_004628.4:c.1769T>G , LRG_472t1:c.1769T>G
|
NP_004619.3:p.Met590Arg
|
|
NR_027299.1:n.1749T>G
|
|
|
XM_011534092.1:c.1769T>G
|
XP_011532394.1:p.Met590Arg
|
|
XM_011534093.1:c.1769T>G
|
XP_011532395.1:p.Met590Arg
|
|
NM_001354726.1:c.1190T>G
|
NP_001341655.1:p.Met397Arg
|
|
NM_001354727.1:c.1769T>G
|
NP_001341656.1:p.Met590Arg
|
|
NM_001354729.1:c.1751T>G
|
NP_001341658.1:p.Met584Arg
|
|
NM_001354730.1:c.1626+143T>G
|
NP_001341659.1:n.1626+143T>G
|
|
NR_148950.1:n.1873T>G
|
|
|
NR_148951.1:n.1749T>G
|
|
|
XR_001740256.2:n.1802T>G
|
|
|
XR_002959580.1:n.1802T>G
|
|
|
XR_002959581.1:n.1802T>G
|
|
|
NM_001354727.2:c.1769T>G
|
NP_001341656.1:p.Met590Arg
|
|
NM_004628.5:c.1769T>G
MANE Select
|
NP_004619.3:p.Met590Arg
|
|
NR_148950.2:n.1802T>G
|
|
|
NR_148951.2:n.1678T>G
|
|
|
NM_001354726.2:c.1190T>G
|
NP_001341655.1:p.Met397Arg
|
|
NM_001354729.2:c.1751T>G
|
NP_001341658.1:p.Met584Arg
|
|
NM_001354730.2:c.1626+143T>G
|
NP_001341659.1:n.1626+143T>G
|
|