ENST00000285021.12:c.2213C>G
MANE Select
|
ENSP00000285021.8:p.Thr738Arg
|
|
ENST00000285021.11:c.2213C>G
|
ENSP00000285021.7:p.Thr738Arg
|
|
ENST00000427795.2:n.78C>G
|
|
|
ENST00000476581.6:c.*1666C>G
|
ENSP00000424548.1:n.*1666C>G
|
|
NM_004628.4:c.2213C>G , LRG_472t1:c.2213C>G
|
NP_004619.3:p.Thr738Arg
|
|
NR_027299.1:n.2193C>G
|
|
|
XM_011534092.1:c.2213C>G
|
XP_011532394.1:p.Thr738Arg
|
|
NM_001354726.1:c.1634C>G
|
NP_001341655.1:p.Thr545Arg
|
|
NM_001354727.1:c.2207C>G
|
NP_001341656.1:p.Thr736Arg
|
|
NM_001354729.1:c.2195C>G
|
NP_001341658.1:p.Thr732Arg
|
|
NM_001354730.1:c.1967C>G
|
NP_001341659.1:p.Thr656Arg
|
|
NR_148950.1:n.2156C>G
|
|
|
NR_148951.1:n.2032C>G
|
|
|
XR_001740256.2:n.2246C>G
|
|
|
XR_002959580.1:n.2246C>G
|
|
|
XR_002959581.1:n.3863C>G
|
|
|
NM_001354727.2:c.2207C>G
|
NP_001341656.1:p.Thr736Arg
|
|
NM_004628.5:c.2213C>G
MANE Select
|
NP_004619.3:p.Thr738Arg
|
|
NR_148950.2:n.2085C>G
|
|
|
NR_148951.2:n.1961C>G
|
|
|
NM_001354726.2:c.1634C>G
|
NP_001341655.1:p.Thr545Arg
|
|
NM_001354729.2:c.2195C>G
|
NP_001341658.1:p.Thr732Arg
|
|
NM_001354730.2:c.1967C>G
|
NP_001341659.1:p.Thr656Arg
|
|