ENST00000382762.8:c.*2338_*2341delinsCAAT
MANE Select
|
ENSP00000372210.3:n.*2338_*2341delinsCAAT
|
|
ENST00000325147.13:c.*2506_*2509delinsCAAT
|
ENSP00000339093.7:n.*2506_*2509delinsCAAT
|
|
ENST00000382762.7:c.*2338_*2341delinsCAAT
|
ENSP00000372210.3:n.*2338_*2341delinsCAAT
|
|
ENST00000410108.5:c.168+2647_168+2650delinsCAAT
|
ENSP00000386558.1:n.168+2647_168+2650delinsCAAT
|
|
NM_001098787.1:c.*2338_*2341delinsCAAT
|
NP_001092257.1:n.*2338_*2341delinsCAAT
|
|
NM_016526.4:c.*2506_*2509delinsCAAT
|
NP_057610.2:n.*2506_*2509delinsCAAT
|
|
NM_001098787.2:c.*2338_*2341delinsCAAT
MANE Select
|
NP_001092257.1:n.*2338_*2341delinsCAAT
|
|
NM_016526.5:c.*2506_*2509delinsCAAT
|
NP_057610.2:n.*2506_*2509delinsCAAT
|
|