ENST00000289575.10:c.1476C>G
MANE Select
|
ENSP00000289575.5:p.Ala492=
|
|
ENST00000289575.9:c.1476C>G
|
ENSP00000289575.5:p.Ala492=
|
|
ENST00000428359.6:c.1410C>G
|
ENSP00000388912.2:p.Ala470=
|
|
ENST00000454962.6:c.795C>G
|
ENSP00000389653.2:p.Ala265=
|
|
ENST00000525650.5:c.1044C>G
|
ENSP00000436324.1:p.Ala348=
|
|
ENST00000528108.1:n.282C>G
|
|
|
ENST00000530012.1:n.303C>G
|
|
|
ENST00000531756.5:n.1023C>G
|
|
|
ENST00000532236.5:c.1128C>G
|
ENSP00000434112.1:p.Ala376=
|
|
NM_001145211.2:c.1410C>G
|
NP_001138683.1:p.Ala470=
|
|
NM_001145212.2:c.1044C>G
|
NP_001138684.1:p.Ala348=
|
|
NM_007256.4:c.1476C>G
|
NP_009187.1:p.Ala492=
|
|
XM_017017157.1:c.1482C>G
|
XP_016872646.1:p.Ala494=
|
|
NM_001145211.3:c.1410C>G
|
NP_001138683.1:p.Ala470=
|
|
NM_001145212.3:c.1044C>G
|
NP_001138684.1:p.Ala348=
|
|
NM_007256.5:c.1476C>G
MANE Select
|
NP_009187.1:p.Ala492=
|
|