ENST00000360215.3:c.*181T>C
MANE Select
|
ENSP00000353346.1:n.*181T>C
|
|
ENST00000496656.2:n.578+3326T>C
|
|
|
ENST00000651132.1:c.*181T>C
|
ENSP00000498322.1:n.*181T>C
|
|
ENST00000651676.1:c.*16+3683T>C
|
ENSP00000498699.1:n.*16+3683T>C
|
|
ENST00000651994.1:c.*261T>C
|
ENSP00000498310.1:n.*261T>C
|
|
ENST00000652718.1:c.508+3683T>C
|
ENSP00000498866.1:n.508+3683T>C
|
|
ENST00000360215.2:c.*181T>C
|
ENSP00000353346.1:n.*181T>C
|
|
ENST00000496656.1:n.812+3326T>C
|
|
|
NM_182548.3:c.*181T>C
|
NP_872354.1:n.*181T>C
|
|
XM_011514403.1:c.*181T>C
|
XP_011512705.1:n.*181T>C
|
|
NM_182548.4:c.*181T>C
MANE Select
|
NP_872354.1:n.*181T>C
|
|