ENST00000455537.7:c.788G>A
MANE Select
|
ENSP00000408979.2:p.Gly263Asp
|
|
ENST00000674619.1:c.788G>A
|
ENSP00000502270.1:p.Gly263Asp
|
|
ENST00000676457.1:c.683G>A
|
ENSP00000501588.1:p.Gly228Asp
|
|
ENST00000286452.5:c.521G>A
|
ENSP00000286452.5:p.Gly174Asp
|
|
ENST00000455537.6:c.788G>A
|
ENSP00000408979.2:p.Gly263Asp
|
|
NM_004984.2:c.788G>A
|
NP_004975.2:p.Gly263Asp
|
|
NM_001354705.1:c.521G>A
|
NP_001341634.1:p.Gly174Asp
|
|
NM_004984.3:c.788G>A
|
NP_004975.2:p.Gly263Asp
|
|
XR_002957324.1:n.1021G>A
|
|
|
NM_004984.4:c.788G>A
MANE Select
|
NP_004975.2:p.Gly263Asp
|
|
NM_001354705.2:c.521G>A
|
NP_001341634.1:p.Gly174Asp
|
|