ENST00000405440.7:c.*1264C>T
MANE Select
|
ENSP00000384152.3:n.*1264C>T
|
|
ENST00000310346.8:c.*1264C>T
|
ENSP00000309913.4:n.*1264C>T
|
|
ENST00000349716.9:c.*1264C>T
|
ENSP00000337723.5:n.*1264C>T
|
|
NM_000192.3:c.*1264C>T , LRG_670t1:c.*1264C>T
|
NP_000183.2:n.*1264C>T
|
|
NM_080717.2:c.*1264C>T
|
NP_542448.1:n.*1264C>T
|
|
NM_181486.2:c.*1264C>T
|
NP_852259.1:n.*1264C>T
|
|
XM_017019912.1:c.*1264C>T
|
XP_016875401.1:n.*1264C>T
|
|
NM_080717.3:c.*1264C>T
|
NP_542448.1:n.*1264C>T
|
|
NM_181486.4:c.*1264C>T
MANE Select
|
NP_852259.1:n.*1264C>T
|
|
NM_080717.4:c.*1264C>T
|
NP_542448.1:n.*1264C>T
|
|