ENST00000682424.1:c.1133T>C
|
ENSP00000507321.1:p.Phe378Ser
|
|
ENST00000299427.12:c.1247T>C
MANE Select
|
ENSP00000299427.6:p.Phe416Ser
|
|
ENST00000436873.7:c.484T>C
|
|
|
ENST00000524924.2:n.367T>C
|
|
|
ENST00000533371.6:c.518T>C
|
ENSP00000437066.1:p.Phe173Ser
|
|
ENST00000642892.1:c.518T>C
|
ENSP00000494165.1:p.Phe173Ser
|
|
ENST00000643342.1:c.320T>C
|
|
|
ENST00000643439.1:c.*987T>C
|
ENSP00000495849.1:n.*987T>C
|
|
ENST00000643479.1:n.1433T>C
|
|
|
ENST00000643516.1:c.756T>C
|
|
|
ENST00000644218.1:c.1058T>C
|
ENSP00000493574.1:p.Phe353Ser
|
|
ENST00000644683.1:c.*700T>C
|
ENSP00000494085.1:n.*700T>C
|
|
ENST00000644810.1:c.968T>C
|
ENSP00000495895.1:p.Phe323Ser
|
|
ENST00000644831.1:n.1423T>C
|
|
|
ENST00000644933.1:c.*113T>C
|
ENSP00000496133.1:n.*113T>C
|
|
ENST00000645285.1:c.*113T>C
|
ENSP00000495058.1:n.*113T>C
|
|
ENST00000645331.1:n.2452T>C
|
|
|
ENST00000645620.1:c.518T>C
|
ENSP00000493657.1:p.Phe173Ser
|
|
ENST00000646691.1:n.1022T>C
|
|
|
ENST00000646777.1:n.1580T>C
|
|
|
ENST00000647016.1:n.1727T>C
|
|
|
ENST00000647152.1:c.518T>C
|
ENSP00000495893.1:p.Phe173Ser
|
|
ENST00000647209.1:c.*1116T>C
|
ENSP00000495558.1:n.*1116T>C
|
|
ENST00000647346.1:n.2267T>C
|
|
|
ENST00000299427.10:c.1247T>C
|
ENSP00000299427.6:p.Phe416Ser
|
|
ENST00000524611.1:n.13T>C
|
|
|
ENST00000524924.1:n.202T>C
|
|
|
ENST00000532191.1:n.300T>C
|
|
|
ENST00000533371.5:c.518T>C
|
ENSP00000437066.1:p.Phe173Ser
|
|
ENST00000611494.4:c.1247T>C
|
ENSP00000484546.1:p.Phe416Ser
|
|
NM_000391.3:c.1247T>C
|
NP_000382.3:p.Phe416Ser
|
|
NM_000391.4:c.1247T>C
MANE Select
|
NP_000382.3:p.Phe416Ser
|
|