ENST00000594045.2:c.*386C>G
|
ENSP00000472329.2:n.*386C>G
|
|
ENST00000594442.2:c.421C>G
|
ENSP00000471239.2:p.Gln141Glu
|
|
ENST00000597629.3:c.403C>G
MANE Select
|
ENSP00000469647.2:p.Gln135Glu
|
|
ENST00000652583.1:n.452C>G
|
|
|
ENST00000594045.1:c.*386C>G
|
ENSP00000472329.1:n.*386C>G
|
|
ENST00000594442.1:c.452C>G
|
|
|
ENST00000597629.1:c.421C>G
|
ENSP00000469647.1:p.Gln141Glu
|
|
ENST00000600033.1:c.422C>G
|
|
|
NM_003407.3:c.421C>G
|
NP_003398.2:p.Gln141Glu
|
|
NM_003407.4:c.403C>G
|
NP_003398.3:p.Gln135Glu
|
|
NM_003407.5:c.403C>G
MANE Select
|
NP_003398.3:p.Gln135Glu
|
|