ENST00000330540.7:c.*1260G>A
MANE Select
|
ENSP00000332049.2:n.*1260G>A
|
|
ENST00000264468.9:c.*1260G>A
|
ENSP00000264468.6:n.*1260G>A
|
|
ENST00000330540.6:c.*1260G>A
|
ENSP00000332049.2:n.*1260G>A
|
|
NM_001206924.1:c.*1258G>A
|
NP_001193853.1:n.*1258G>A
|
|
NM_001206925.1:c.*1258G>A
|
NP_001193854.1:n.*1258G>A
|
|
NM_006889.4:c.*1258G>A
|
NP_008820.3:n.*1258G>A
|
|
NM_175862.4:c.*1258G>A
|
NP_787058.4:n.*1258G>A
|
|
NM_176892.1:c.*1258G>A
|
NP_795711.1:n.*1258G>A
|
|
NM_175862.5:c.*1260G>A
MANE Select
|
NP_787058.5:n.*1260G>A
|
|
NM_001206924.2:c.*1260G>A
|
NP_001193853.2:n.*1260G>A
|
|
NM_001206925.2:c.*1260G>A
|
NP_001193854.2:n.*1260G>A
|
|
NM_006889.5:c.*1260G>A
|
NP_008820.4:n.*1260G>A
|
|
NM_176892.2:c.*1260G>A
|
NP_795711.2:n.*1260G>A
|
|