ENST00000229771.11:c.1384C>G
MANE Select
|
ENSP00000229771.6:p.His462Asp
|
|
ENST00000229771.10:c.1384C>G
|
ENSP00000229771.6:p.His462Asp
|
|
ENST00000322263.8:c.1225C>G
|
ENSP00000319414.4:p.His409Asp
|
|
ENST00000495781.1:n.560C>G
|
|
|
ENST00000614066.4:c.1378C>G
|
ENSP00000477534.1:p.His460Asp
|
|
NM_001289395.1:c.1225C>G
|
NP_001276324.1:p.His409Asp
|
|
NM_003322.4:c.1384C>G
|
NP_003313.3:p.His462Asp
|
|
NM_003322.5:c.1384C>G
|
NP_003313.3:p.His462Asp
|
|
NM_003322.6:c.1384C>G
MANE Select
|
NP_003313.3:p.His462Asp
|
|
NM_001289395.2:c.1225C>G
|
NP_001276324.1:p.His409Asp
|
|