ENST00000341049.7:c.*1039G>A
MANE Select
|
ENSP00000339191.2:n.*1039G>A
|
|
ENST00000405348.6:c.*1039G>A
|
ENSP00000384348.1:n.*1039G>A
|
|
ENST00000341049.6:c.*1039G>A
|
ENSP00000339191.2:n.*1039G>A
|
|
ENST00000393467.1:c.*1039G>A
|
ENSP00000377110.1:n.*1039G>A
|
|
ENST00000405348.5:c.*1039G>A
|
ENSP00000384348.1:n.*1039G>A
|
|
ENST00000614113.4:c.*1039G>A
|
ENSP00000479447.1:n.*1039G>A
|
|
NM_001172895.1:c.*1039G>A
|
NP_001166366.1:n.*1039G>A
|
|
NM_001172896.1:c.*1039G>A
|
NP_001166367.1:n.*1039G>A
|
|
NM_001172897.1:c.*1039G>A
|
NP_001166368.1:n.*1039G>A
|
|
NM_001753.4:c.*1039G>A
|
NP_001744.2:n.*1039G>A
|
|
NM_001753.5:c.*1039G>A
MANE Select
|
NP_001744.2:n.*1039G>A
|
|
NM_001172896.2:c.*1039G>A
|
NP_001166367.1:n.*1039G>A
|
|
NM_001172897.2:c.*1039G>A
|
NP_001166368.1:n.*1039G>A
|
|