ENST00000360215.3:c.*895T>C
MANE Select
|
ENSP00000353346.1:n.*895T>C
|
|
ENST00000496656.2:n.578+4040T>C
|
|
|
ENST00000651132.1:c.*895T>C
|
ENSP00000498322.1:n.*895T>C
|
|
ENST00000651676.1:c.*16+4397T>C
|
ENSP00000498699.1:n.*16+4397T>C
|
|
ENST00000651994.1:c.*975T>C
|
ENSP00000498310.1:n.*975T>C
|
|
ENST00000652718.1:c.508+4397T>C
|
ENSP00000498866.1:n.508+4397T>C
|
|
ENST00000360215.2:c.*895T>C
|
ENSP00000353346.1:n.*895T>C
|
|
ENST00000496656.1:n.812+4040T>C
|
|
|
NM_182548.3:c.*895T>C
|
NP_872354.1:n.*895T>C
|
|
NM_182548.4:c.*895T>C
MANE Select
|
NP_872354.1:n.*895T>C
|
|