|
NM_003718.5:c.2511T>A
MANE Select
|
NP_003709.3:p.Asp837Glu
|
|
ENST00000181839.10:c.2511T>A
MANE Select
|
ENSP00000181839.4:p.Asp837Glu
|
|
NM_003718.4:c.2511T>A
|
NP_003709.3:p.Asp837Glu
|
|
NM_031267.3:c.2511T>A
|
NP_112557.2:p.Asp837Glu
|
|
ENST00000181839.8:c.2511T>A
|
ENSP00000181839.4:p.Asp837Glu
|
|
ENST00000340829.10:c.2511T>A
|
ENSP00000340557.5:p.Asp837Glu
|
|
ENST00000340829.9:c.2511T>A
|
ENSP00000340557.5:p.Asp837Glu
|
|
ENST00000484589.1:n.1063T>A
|
|
|
ENST00000484589.2:c.1063T>A
|
|
|
ENST00000611390.1:c.669T>A
|
ENSP00000484610.1:p.Asp223Glu
|
|
ENST00000613626.4:c.669T>A
|
ENSP00000480835.1:p.Asp223Glu
|
|
ENST00000642592.1:c.64T>A
|
|
|
ENST00000643859.1:c.1402T>A
|
|
|
ENST00000643915.1:c.825T>A
|
ENSP00000496187.1:p.Asp275Glu
|
|
ENST00000645470.1:c.441T>A
|
ENSP00000495036.1:p.Asp147Glu
|
|
ENST00000646039.1:c.1851T>A
|
ENSP00000494168.1:p.Asp617Glu
|
|
ENST00000647453.1:n.1580T>A
|
|
|
ENST00000700485.1:n.247T>A
|
|
|
ENST00000700486.1:n.285T>A
|
|
|
ENST00000700487.1:n.253T>A
|
|
|
XM_011515597.1:c.2511T>A
|
XP_011513899.1:p.Asp837Glu
|
|
XM_011515597.3:c.2511T>A
|
XP_011513899.1:p.Asp837Glu
|
|
XM_011515598.1:c.2511T>A
|
XP_011513900.1:p.Asp837Glu
|
|
XM_017012750.2:c.2511T>A
|
XP_016868239.1:p.Asp837Glu
|
|
XM_017012751.2:c.2511T>A
|
XP_016868240.1:p.Asp837Glu
|