ENST00000290866.10:c.3791T>C
MANE Select
|
ENSP00000290866.4:p.Phe1264Ser
|
|
ENST00000290863.10:c.2069T>C
|
ENSP00000290863.6:p.Phe690Ser
|
|
ENST00000290866.9:c.3791T>C
|
ENSP00000290866.4:p.Phe1264Ser
|
|
ENST00000413513.7:c.1946T>C
|
ENSP00000392247.3:p.Phe649Ser
|
|
ENST00000428043.5:c.*213T>C
|
ENSP00000397593.2:n.*213T>C
|
|
ENST00000577647.2:c.1969+251T>C
|
ENSP00000464149.1:n.1969+251T>C
|
|
ENST00000578839.5:c.*1546T>C
|
ENSP00000462110.2:n.*1546T>C
|
|
ENST00000579314.5:c.*1520T>C
|
ENSP00000462599.1:n.*1520T>C
|
|
NM_000789.3:c.3791T>C
|
NP_000780.1:p.Phe1264Ser
|
|
NM_001178057.1:c.1946T>C
|
NP_001171528.1:p.Phe649Ser
|
|
NM_152830.2:c.2069T>C
|
NP_690043.1:p.Phe690Ser
|
|
XM_005257110.1:c.3242T>C
|
XP_005257167.1:p.Phe1081Ser
|
|
XM_006721737.2:c.2129T>C
|
XP_006721800.2:p.Phe710Ser
|
|
XM_006721737.3:c.2129T>C
|
XP_006721800.2:p.Phe710Ser
|
|
NM_000789.4:c.3791T>C
MANE Select
|
NP_000780.1:p.Phe1264Ser
|
|
NM_001178057.2:c.1946T>C
|
NP_001171528.1:p.Phe649Ser
|
|
NM_152830.3:c.2069T>C
|
NP_690043.1:p.Phe690Ser
|
|
NM_001382700.1:c.3224T>C
|
NP_001369629.1:p.Phe1075Ser
|
|
NM_001382701.1:c.2939T>C
|
NP_001369630.1:p.Phe980Ser
|
|
NM_001382702.1:c.1406T>C
|
NP_001369631.1:p.Phe469Ser
|
|
NR_168483.1:n.2169T>C
|
|
|