ENST00000360215.3:c.*802T>C
MANE Select
|
ENSP00000353346.1:n.*802T>C
|
|
ENST00000496656.2:n.578+3947T>C
|
|
|
ENST00000651132.1:c.*802T>C
|
ENSP00000498322.1:n.*802T>C
|
|
ENST00000651676.1:c.*16+4304T>C
|
ENSP00000498699.1:n.*16+4304T>C
|
|
ENST00000651994.1:c.*882T>C
|
ENSP00000498310.1:n.*882T>C
|
|
ENST00000652718.1:c.508+4304T>C
|
ENSP00000498866.1:n.508+4304T>C
|
|
ENST00000360215.2:c.*802T>C
|
ENSP00000353346.1:n.*802T>C
|
|
ENST00000496656.1:n.812+3947T>C
|
|
|
NM_182548.3:c.*802T>C
|
NP_872354.1:n.*802T>C
|
|
NM_182548.4:c.*802T>C
MANE Select
|
NP_872354.1:n.*802T>C
|
|