ENST00000290866.10:c.3790T>G
MANE Select
|
ENSP00000290866.4:p.Phe1264Val
|
|
ENST00000290863.10:c.2068T>G
|
ENSP00000290863.6:p.Phe690Val
|
|
ENST00000290866.9:c.3790T>G
|
ENSP00000290866.4:p.Phe1264Val
|
|
ENST00000413513.7:c.1945T>G
|
ENSP00000392247.3:p.Phe649Val
|
|
ENST00000428043.5:c.*212T>G
|
ENSP00000397593.2:n.*212T>G
|
|
ENST00000577647.2:c.1969+250T>G
|
ENSP00000464149.1:n.1969+250T>G
|
|
ENST00000578839.5:c.*1545T>G
|
ENSP00000462110.2:n.*1545T>G
|
|
ENST00000579314.5:c.*1519T>G
|
ENSP00000462599.1:n.*1519T>G
|
|
NM_000789.3:c.3790T>G
|
NP_000780.1:p.Phe1264Val
|
|
NM_001178057.1:c.1945T>G
|
NP_001171528.1:p.Phe649Val
|
|
NM_152830.2:c.2068T>G
|
NP_690043.1:p.Phe690Val
|
|
XM_005257110.1:c.3241T>G
|
XP_005257167.1:p.Phe1081Val
|
|
XM_006721737.2:c.2128T>G
|
XP_006721800.2:p.Phe710Val
|
|
XM_006721737.3:c.2128T>G
|
XP_006721800.2:p.Phe710Val
|
|
NM_000789.4:c.3790T>G
MANE Select
|
NP_000780.1:p.Phe1264Val
|
|
NM_001178057.2:c.1945T>G
|
NP_001171528.1:p.Phe649Val
|
|
NM_152830.3:c.2068T>G
|
NP_690043.1:p.Phe690Val
|
|
NM_001382700.1:c.3223T>G
|
NP_001369629.1:p.Phe1075Val
|
|
NM_001382701.1:c.2938T>G
|
NP_001369630.1:p.Phe980Val
|
|
NM_001382702.1:c.1405T>G
|
NP_001369631.1:p.Phe469Val
|
|
NR_168483.1:n.2168T>G
|
|
|