ENST00000290866.10:c.3842T>G
MANE Select
|
ENSP00000290866.4:p.Phe1281Cys
|
|
ENST00000290863.10:c.2120T>G
|
ENSP00000290863.6:p.Phe707Cys
|
|
ENST00000290866.9:c.3842T>G
|
ENSP00000290866.4:p.Phe1281Cys
|
|
ENST00000413513.7:c.1997T>G
|
ENSP00000392247.3:p.Phe666Cys
|
|
ENST00000428043.5:c.*264T>G
|
ENSP00000397593.2:n.*264T>G
|
|
ENST00000577647.2:c.1969+302T>G
|
ENSP00000464149.1:n.1969+302T>G
|
|
ENST00000578839.5:c.*1597T>G
|
ENSP00000462110.2:n.*1597T>G
|
|
ENST00000579314.5:c.*1571T>G
|
ENSP00000462599.1:n.*1571T>G
|
|
NM_000789.3:c.3842T>G
|
NP_000780.1:p.Phe1281Cys
|
|
NM_001178057.1:c.1997T>G
|
NP_001171528.1:p.Phe666Cys
|
|
NM_152830.2:c.2120T>G
|
NP_690043.1:p.Phe707Cys
|
|
XM_005257110.1:c.3293T>G
|
XP_005257167.1:p.Phe1098Cys
|
|
XM_006721737.2:c.2180T>G
|
XP_006721800.2:p.Phe727Cys
|
|
XM_006721737.3:c.2180T>G
|
XP_006721800.2:p.Phe727Cys
|
|
NM_000789.4:c.3842T>G
MANE Select
|
NP_000780.1:p.Phe1281Cys
|
|
NM_001178057.2:c.1997T>G
|
NP_001171528.1:p.Phe666Cys
|
|
NM_152830.3:c.2120T>G
|
NP_690043.1:p.Phe707Cys
|
|
NM_001382700.1:c.3275T>G
|
NP_001369629.1:p.Phe1092Cys
|
|
NM_001382701.1:c.2990T>G
|
NP_001369630.1:p.Phe997Cys
|
|
NM_001382702.1:c.1457T>G
|
NP_001369631.1:p.Phe486Cys
|
|
NR_168483.1:n.2220T>G
|
|
|