ENST00000293778.12:c.*2C>A
MANE Select
|
ENSP00000293778.7:n.*2C>A
|
|
ENST00000574412.6:c.*2C>A
|
ENSP00000459592.2:n.*2C>A
|
|
ENST00000293778.10:c.*2C>A
|
ENSP00000293778.6:n.*2C>A
|
|
ENST00000574412.5:c.*2C>A
|
ENSP00000459592.1:n.*2C>A
|
|
ENST00000575168.1:n.598C>A
|
|
|
ENST00000576153.5:n.558C>A
|
|
|
NM_001100812.1:c.*2C>A
|
NP_001094282.1:n.*2C>A
|
|
NM_022059.3:c.*2C>A
|
NP_071342.2:n.*2C>A
|
|
NM_022059.4:c.*2C>A
|
NP_071342.2:n.*2C>A
|
|
NM_001100812.2:c.*2C>A
|
NP_001094282.2:n.*2C>A
|
|
NM_001386809.1:c.*2C>A
MANE Select
|
NP_001373738.1:n.*2C>A
|
|