ENST00000341529.8:c.1570T>G
MANE Select
|
ENSP00000344115.3:p.Phe524Val
|
|
ENST00000649567.1:c.1570T>G
|
ENSP00000497290.1:p.Phe524Val
|
|
ENST00000341529.7:c.1570T>G
|
ENSP00000344115.3:p.Phe524Val
|
|
ENST00000539168.1:c.-114T>G
|
ENSP00000461880.1:n.-114T>G
|
|
ENST00000565334.5:c.*693T>G
|
ENSP00000456028.1:n.*693T>G
|
|
ENST00000614547.4:c.1225T>G
|
ENSP00000479381.1:p.Phe409Val
|
|
NM_001795.3:c.1570T>G
|
NP_001786.2:p.Phe524Val
|
|
XM_011522801.1:c.1597T>G
|
XP_011521103.1:p.Phe533Val
|
|
NM_001795.4:c.1570T>G
|
NP_001786.2:p.Phe524Val
|
|
XM_011522801.2:c.1597T>G
|
XP_011521103.1:p.Phe533Val
|
|
XM_024450133.1:c.1597T>G
|
XP_024305901.1:p.Phe533Val
|
|
NM_001795.5:c.1570T>G
MANE Select
|
NP_001786.2:p.Phe524Val
|
|