ENST00000392583.7:c.*1228A>T
MANE Select
|
ENSP00000376362.3:n.*1228A>T
|
|
ENST00000679877.1:c.*3981A>T
|
ENSP00000506110.1:n.*3981A>T
|
|
ENST00000680122.1:c.*2503A>T
|
ENSP00000505194.1:n.*2503A>T
|
|
ENST00000680138.1:c.*2120A>T
|
ENSP00000506262.1:n.*2120A>T
|
|
ENST00000680898.1:n.3825A>T
|
|
|
ENST00000681023.1:n.3742A>T
|
|
|
ENST00000342315.8:c.2159A>T
|
ENSP00000342278.4:p.Ter720Leu
|
|
ENST00000392583.6:c.*1228A>T
|
ENSP00000376362.2:n.*1228A>T
|
|
ENST00000620097.1:c.2158-2A>T
|
ENSP00000483679.1:n.2158-2A>T
|
|
NM_002535.2:c.*1228A>T
|
NP_002526.2:n.*1228A>T
|
|
NM_016817.2:c.2159A>T
|
NP_058197.2:p.Ter720Leu
|
|
XM_011538415.1:c.2069A>T
|
XP_011536717.1:p.Ter690Leu
|
|
XR_001748725.2:n.3894A>T
|
|
|
NM_002535.3:c.*1228A>T
MANE Select
|
NP_002526.2:n.*1228A>T
|
|
NM_016817.3:c.2159A>T
|
NP_058197.2:p.Ter720Leu
|
|