ENST00000309539.8:c.*916A>G
MANE Select
|
ENSP00000309124.3:n.*916A>G
|
|
ENST00000309539.7:c.*916A>G
|
ENSP00000309124.3:n.*916A>G
|
|
NM_001172632.1:c.*1052A>G
|
NP_001166103.1:n.*1052A>G
|
|
NM_001172633.1:c.*1052A>G
|
NP_001166104.1:n.*1052A>G
|
|
NM_002543.3:c.*916A>G
|
NP_002534.1:n.*916A>G
|
|
XM_011520682.1:c.*916A>G
|
XP_011518984.1:n.*916A>G
|
|
XM_011520683.1:c.*1068A>G
|
XP_011518985.1:n.*1068A>G
|
|
NM_002543.4:c.*916A>G
MANE Select
|
NP_002534.1:n.*916A>G
|
|
NM_001172632.2:c.*1052A>G
|
NP_001166103.1:n.*1052A>G
|
|
NM_001172633.2:c.*1052A>G
|
NP_001166104.1:n.*1052A>G
|
|