ENST00000368666.7:c.*27T>A
MANE Select
|
ENSP00000357655.4:n.*27T>A
|
|
ENST00000639360.1:c.993T>A
|
ENSP00000491774.1:n.993T>A
|
|
ENST00000230529.9:c.*27T>A
|
ENSP00000230529.5:n.*27T>A
|
|
ENST00000361714.5:c.*27T>A
|
ENSP00000354734.2:n.*27T>A
|
|
ENST00000368664.7:c.*496T>A
|
ENSP00000357653.3:n.*496T>A
|
|
ENST00000368666.6:c.*27T>A
|
ENSP00000357655.3:n.*27T>A
|
|
ENST00000409166.5:c.*27T>A
|
ENSP00000386467.1:n.*27T>A
|
|
ENST00000454589.5:c.*496T>A
|
ENSP00000395928.1:n.*496T>A
|
|
ENST00000604763.5:c.*27T>A
|
ENSP00000473777.1:n.*27T>A
|
|
ENST00000613648.1:n.927T>A
|
|
|
ENST00000620524.3:n.1023T>A
|
|
|
NM_003880.3:c.*27T>A
|
NP_003871.1:n.*27T>A
|
|
NM_198239.1:c.*27T>A
|
NP_937882.1:n.*27T>A
|
|
NR_125353.1:n.1346T>A
|
|
|
NR_125354.1:n.1266T>A
|
|
|
XM_011536220.1:c.*27T>A
|
XP_011534522.1:n.*27T>A
|
|
XM_011536221.1:c.*496T>A
|
XP_011534523.1:n.*496T>A
|
|
XM_011536223.1:c.*27T>A
|
XP_011534525.1:n.*27T>A
|
|
XM_011536223.3:c.*27T>A
|
XP_011534525.1:n.*27T>A
|
|
XR_001743705.1:n.1694T>A
|
|
|
NM_003880.4:c.*27T>A
|
NP_003871.1:n.*27T>A
|
|
NM_198239.2:c.*27T>A
MANE Select
|
NP_937882.2:n.*27T>A
|
|
NR_125353.2:n.1410T>A
|
|
|
NR_125354.3:n.1237T>A
|
|
|