ENST00000547314.6:c.*4388A>G
|
ENSP00000449934.2:n.*4388A>G
|
|
ENST00000552573.7:c.*4388A>G
|
ENSP00000447182.3:n.*4388A>G
|
|
ENST00000374994.9:c.*4388A>G
MANE Select
|
ENSP00000364133.4:n.*4388A>G
|
|
ENST00000374994.8:c.*4388A>G
|
ENSP00000364133.4:n.*4388A>G
|
|
NM_001130916.1:c.*4388A>G
|
NP_001124388.1:n.*4388A>G
|
|
NM_001130916.2:c.*4388A>G
|
NP_001124388.1:n.*4388A>G
|
|
NM_001306210.1:c.*4388A>G
|
NP_001293139.1:n.*4388A>G
|
|
NM_004612.2:c.*4388A>G
|
NP_004603.1:n.*4388A>G
|
|
NM_004612.3:c.*4388A>G
|
NP_004603.1:n.*4388A>G
|
|
XM_011518948.1:c.*4388A>G
|
XP_011517250.1:n.*4388A>G
|
|
XM_011518949.1:c.*4388A>G
|
XP_011517251.1:n.*4388A>G
|
|
XM_011518950.1:c.*4388A>G
|
XP_011517252.1:n.*4388A>G
|
|
NM_004612.4:c.*4388A>G
MANE Select
|
NP_004603.1:n.*4388A>G
|
|
NM_001130916.3:c.*4388A>G
|
NP_001124388.1:n.*4388A>G
|
|
NM_001306210.2:c.*4388A>G
|
NP_001293139.1:n.*4388A>G
|
|