ENST00000290866.10:c.3832C>T
MANE Select
|
ENSP00000290866.4:p.Gln1278Ter
|
|
ENST00000290863.10:c.2110C>T
|
ENSP00000290863.6:p.Gln704Ter
|
|
ENST00000290866.9:c.3832C>T
|
ENSP00000290866.4:p.Gln1278Ter
|
|
ENST00000413513.7:c.1987C>T
|
ENSP00000392247.3:p.Gln663Ter
|
|
ENST00000428043.5:c.*254C>T
|
ENSP00000397593.2:n.*254C>T
|
|
ENST00000577647.2:c.1969+292C>T
|
ENSP00000464149.1:n.1969+292C>T
|
|
ENST00000578839.5:c.*1587C>T
|
ENSP00000462110.2:n.*1587C>T
|
|
ENST00000579314.5:c.*1561C>T
|
ENSP00000462599.1:n.*1561C>T
|
|
NM_000789.3:c.3832C>T
|
NP_000780.1:p.Gln1278Ter
|
|
NM_001178057.1:c.1987C>T
|
NP_001171528.1:p.Gln663Ter
|
|
NM_152830.2:c.2110C>T
|
NP_690043.1:p.Gln704Ter
|
|
XM_005257110.1:c.3283C>T
|
XP_005257167.1:p.Gln1095Ter
|
|
XM_006721737.2:c.2170C>T
|
XP_006721800.2:p.Gln724Ter
|
|
XM_006721737.3:c.2170C>T
|
XP_006721800.2:p.Gln724Ter
|
|
NM_000789.4:c.3832C>T
MANE Select
|
NP_000780.1:p.Gln1278Ter
|
|
NM_001178057.2:c.1987C>T
|
NP_001171528.1:p.Gln663Ter
|
|
NM_152830.3:c.2110C>T
|
NP_690043.1:p.Gln704Ter
|
|
NM_001382700.1:c.3265C>T
|
NP_001369629.1:p.Gln1089Ter
|
|
NM_001382701.1:c.2980C>T
|
NP_001369630.1:p.Gln994Ter
|
|
NM_001382702.1:c.1447C>T
|
NP_001369631.1:p.Gln483Ter
|
|
NR_168483.1:n.2210C>T
|
|
|