ENST00000285021.12:c.2396T>A
MANE Select
|
ENSP00000285021.8:p.Phe799Tyr
|
|
ENST00000285021.11:c.2396T>A
|
ENSP00000285021.7:p.Phe799Tyr
|
|
ENST00000427795.2:n.261T>A
|
|
|
ENST00000476581.6:c.*1849T>A
|
ENSP00000424548.1:n.*1849T>A
|
|
NM_004628.4:c.2396T>A , LRG_472t1:c.2396T>A
|
NP_004619.3:p.Phe799Tyr
|
|
NR_027299.1:n.2376T>A
|
|
|
XM_011534092.1:c.2396T>A
|
XP_011532394.1:p.Phe799Tyr
|
|
NM_001354726.1:c.1817T>A
|
NP_001341655.1:p.Phe606Tyr
|
|
NM_001354727.1:c.2390T>A
|
NP_001341656.1:p.Phe797Tyr
|
|
NM_001354729.1:c.2378T>A
|
NP_001341658.1:p.Phe793Tyr
|
|
NM_001354730.1:c.2150T>A
|
NP_001341659.1:p.Phe717Tyr
|
|
NR_148950.1:n.2339T>A
|
|
|
NR_148951.1:n.2215T>A
|
|
|
XR_001740256.2:n.2429T>A
|
|
|
XR_002959580.1:n.2429T>A
|
|
|
XR_002959581.1:n.4046T>A
|
|
|
NM_001354727.2:c.2390T>A
|
NP_001341656.1:p.Phe797Tyr
|
|
NM_004628.5:c.2396T>A
MANE Select
|
NP_004619.3:p.Phe799Tyr
|
|
NR_148950.2:n.2268T>A
|
|
|
NR_148951.2:n.2144T>A
|
|
|
NM_001354726.2:c.1817T>A
|
NP_001341655.1:p.Phe606Tyr
|
|
NM_001354729.2:c.2378T>A
|
NP_001341658.1:p.Phe793Tyr
|
|
NM_001354730.2:c.2150T>A
|
NP_001341659.1:p.Phe717Tyr
|
|