ENST00000285021.12:c.2372T>A
MANE Select
|
ENSP00000285021.8:p.Val791Asp
|
|
ENST00000285021.11:c.2372T>A
|
ENSP00000285021.7:p.Val791Asp
|
|
ENST00000427795.2:n.237T>A
|
|
|
ENST00000476581.6:c.*1825T>A
|
ENSP00000424548.1:n.*1825T>A
|
|
NM_004628.4:c.2372T>A , LRG_472t1:c.2372T>A
|
NP_004619.3:p.Val791Asp
|
|
NR_027299.1:n.2352T>A
|
|
|
XM_011534092.1:c.2372T>A
|
XP_011532394.1:p.Val791Asp
|
|
NM_001354726.1:c.1793T>A
|
NP_001341655.1:p.Val598Asp
|
|
NM_001354727.1:c.2366T>A
|
NP_001341656.1:p.Val789Asp
|
|
NM_001354729.1:c.2354T>A
|
NP_001341658.1:p.Val785Asp
|
|
NM_001354730.1:c.2126T>A
|
NP_001341659.1:p.Val709Asp
|
|
NR_148950.1:n.2315T>A
|
|
|
NR_148951.1:n.2191T>A
|
|
|
XR_001740256.2:n.2405T>A
|
|
|
XR_002959580.1:n.2405T>A
|
|
|
XR_002959581.1:n.4022T>A
|
|
|
NM_001354727.2:c.2366T>A
|
NP_001341656.1:p.Val789Asp
|
|
NM_004628.5:c.2372T>A
MANE Select
|
NP_004619.3:p.Val791Asp
|
|
NR_148950.2:n.2244T>A
|
|
|
NR_148951.2:n.2120T>A
|
|
|
NM_001354726.2:c.1793T>A
|
NP_001341655.1:p.Val598Asp
|
|
NM_001354729.2:c.2354T>A
|
NP_001341658.1:p.Val785Asp
|
|
NM_001354730.2:c.2126T>A
|
NP_001341659.1:p.Val709Asp
|
|