|
NM_004082.5:c.2426A>T
MANE Select
|
NP_004073.2:p.Asp809Val
|
|
ENST00000628224.3:c.2426A>T
MANE Select
|
ENSP00000487279.2:p.Asp809Val
|
|
NM_001135040.2:c.2366A>T
|
NP_001128512.1:p.Asp789Val
|
|
NM_001135040.3:c.2366A>T
|
NP_001128512.1:p.Asp789Val
|
|
NM_001135041.2:c.2024A>T
|
NP_001128513.1:p.Asp675Val
|
|
NM_001135041.3:c.2024A>T
|
NP_001128513.1:p.Asp675Val
|
|
NM_001190836.1:c.2315A>T
|
NP_001177765.1:p.Asp772Val
|
|
NM_001190836.2:c.2315A>T
|
NP_001177765.1:p.Asp772Val
|
|
NM_001190837.1:c.2405A>T
|
NP_001177766.1:p.Asp802Val
|
|
NM_001190837.2:c.2405A>T
|
NP_001177766.1:p.Asp802Val
|
|
NM_001378991.1:c.2375A>T
|
NP_001365920.1:p.Asp792Val
|
|
NM_001378992.1:c.2357A>T
|
NP_001365921.1:p.Asp786Val
|
|
NM_004082.4:c.2426A>T
|
NP_004073.2:p.Asp809Val
|
|
NM_023019.3:c.2024A>T
|
NP_075408.1:p.Asp675Val
|
|
NM_023019.4:c.2024A>T
|
NP_075408.1:p.Asp675Val
|
|
NR_033935.1:n.2627A>T
|
|
|
NR_033935.2:n.2406A>T
|
|
|
ENST00000361874.7:c.2426A>T
|
ENSP00000354791.3:p.Asp809Val
|
|
ENST00000361874.8:c.2426A>T
|
ENSP00000354791.4:p.Asp809Val
|
|
ENST00000394003.7:c.2405A>T
|
ENSP00000377571.3:p.Asp802Val
|
|
ENST00000409240.5:c.2315A>T
|
ENSP00000386406.1:p.Asp772Val
|
|
ENST00000409438.5:c.2024A>T
|
ENSP00000387270.1:p.Asp675Val
|
|
ENST00000409567.7:c.2366A>T
|
ENSP00000386843.3:p.Asp789Val
|
|
ENST00000409868.5:c.2375A>T
|
ENSP00000387327.1:p.Asp792Val
|
|
ENST00000434055.5:c.2315A>T
|
ENSP00000416711.1:p.Asp772Val
|
|
ENST00000466110.5:n.3243A>T
|
|
|
ENST00000495643.1:n.454A>T
|
|
|
ENST00000497666.1:n.96+2477A>T
|
|
|
ENST00000628224.2:c.2375A>T
|
ENSP00000487279.1:p.Asp792Val
|
|
ENST00000633691.1:c.2024A>T
|
ENSP00000487724.1:p.Asp675Val
|
|
ENST00000680606.1:c.2375A>T
|
ENSP00000505612.1:p.Asp792Val
|
