ENST00000290866.10:c.3887A>T
MANE Select
|
ENSP00000290866.4:p.Gln1296Leu
|
|
ENST00000290863.10:c.2165A>T
|
ENSP00000290863.6:p.Gln722Leu
|
|
ENST00000290866.9:c.3887A>T
|
ENSP00000290866.4:p.Gln1296Leu
|
|
ENST00000413513.7:c.2042A>T
|
ENSP00000392247.3:p.Gln681Leu
|
|
ENST00000428043.5:c.*309A>T
|
ENSP00000397593.2:n.*309A>T
|
|
ENST00000577647.2:c.1969+347A>T
|
ENSP00000464149.1:n.1969+347A>T
|
|
ENST00000578839.5:c.*1642A>T
|
ENSP00000462110.2:n.*1642A>T
|
|
ENST00000579314.5:c.*1616A>T
|
ENSP00000462599.1:n.*1616A>T
|
|
NM_000789.3:c.3887A>T
|
NP_000780.1:p.Gln1296Leu
|
|
NM_001178057.1:c.2042A>T
|
NP_001171528.1:p.Gln681Leu
|
|
NM_152830.2:c.2165A>T
|
NP_690043.1:p.Gln722Leu
|
|
XM_005257110.1:c.3338A>T
|
XP_005257167.1:p.Gln1113Leu
|
|
XM_006721737.2:c.2225A>T
|
XP_006721800.2:p.Gln742Leu
|
|
XM_006721737.3:c.2225A>T
|
XP_006721800.2:p.Gln742Leu
|
|
NM_000789.4:c.3887A>T
MANE Select
|
NP_000780.1:p.Gln1296Leu
|
|
NM_001178057.2:c.2042A>T
|
NP_001171528.1:p.Gln681Leu
|
|
NM_152830.3:c.2165A>T
|
NP_690043.1:p.Gln722Leu
|
|
NM_001382700.1:c.3320A>T
|
NP_001369629.1:p.Gln1107Leu
|
|
NM_001382701.1:c.3035A>T
|
NP_001369630.1:p.Gln1012Leu
|
|
NM_001382702.1:c.1502A>T
|
NP_001369631.1:p.Gln501Leu
|
|
NR_168483.1:n.2265A>T
|
|
|