ENST00000285021.12:c.2299A>T
MANE Select
|
ENSP00000285021.8:p.Met767Leu
|
|
ENST00000285021.11:c.2299A>T
|
ENSP00000285021.7:p.Met767Leu
|
|
ENST00000427795.2:n.164A>T
|
|
|
ENST00000476581.6:c.*1752A>T
|
ENSP00000424548.1:n.*1752A>T
|
|
NM_004628.4:c.2299A>T , LRG_472t1:c.2299A>T
|
NP_004619.3:p.Met767Leu
|
|
NR_027299.1:n.2279A>T
|
|
|
XM_011534092.1:c.2299A>T
|
XP_011532394.1:p.Met767Leu
|
|
NM_001354726.1:c.1720A>T
|
NP_001341655.1:p.Met574Leu
|
|
NM_001354727.1:c.2293A>T
|
NP_001341656.1:p.Met765Leu
|
|
NM_001354729.1:c.2281A>T
|
NP_001341658.1:p.Met761Leu
|
|
NM_001354730.1:c.2053A>T
|
NP_001341659.1:p.Met685Leu
|
|
NR_148950.1:n.2242A>T
|
|
|
NR_148951.1:n.2118A>T
|
|
|
XR_001740256.2:n.2332A>T
|
|
|
XR_002959580.1:n.2332A>T
|
|
|
XR_002959581.1:n.3949A>T
|
|
|
NM_001354727.2:c.2293A>T
|
NP_001341656.1:p.Met765Leu
|
|
NM_004628.5:c.2299A>T
MANE Select
|
NP_004619.3:p.Met767Leu
|
|
NR_148950.2:n.2171A>T
|
|
|
NR_148951.2:n.2047A>T
|
|
|
NM_001354726.2:c.1720A>T
|
NP_001341655.1:p.Met574Leu
|
|
NM_001354729.2:c.2281A>T
|
NP_001341658.1:p.Met761Leu
|
|
NM_001354730.2:c.2053A>T
|
NP_001341659.1:p.Met685Leu
|
|