ENST00000258439.8:c.*1873C>A
MANE Select
|
ENSP00000258439.3:n.*1873C>A
|
|
ENST00000258439.7:c.*1873C>A
|
ENSP00000258439.2:n.*1873C>A
|
|
ENST00000432959.1:c.*1873C>A
|
ENSP00000416660.1:n.*1873C>A
|
|
NM_001193304.2:c.*1873C>A
|
NP_001180233.1:n.*1873C>A
|
|
NM_017849.3:c.*1873C>A , LRG_528t1:c.*1873C>A
|
NP_060319.1:n.*1873C>A
|
|
XM_017004450.1:c.*1174C>A
|
XP_016859939.1:n.*1174C>A
|
|
XM_017004452.1:c.*1873C>A
|
XP_016859941.1:n.*1873C>A
|
|
NM_001193304.3:c.*1873C>A
|
NP_001180233.1:n.*1873C>A
|
|
NM_017849.4:c.*1873C>A
MANE Select
|
NP_060319.1:n.*1873C>A
|
|