ENST00000682424.1:c.1246G>T
|
ENSP00000507321.1:p.Ala416Ser
|
|
ENST00000299427.12:c.1360G>T
MANE Select
|
ENSP00000299427.6:p.Ala454Ser
|
|
ENST00000524611.2:n.220G>T
|
|
|
ENST00000524924.2:n.480G>T
|
|
|
ENST00000533371.6:c.631G>T
|
ENSP00000437066.1:p.Ala211Ser
|
|
ENST00000642892.1:c.631G>T
|
ENSP00000494165.1:p.Ala211Ser
|
|
ENST00000643342.1:c.433G>T
|
|
|
ENST00000643439.1:c.*1100G>T
|
ENSP00000495849.1:n.*1100G>T
|
|
ENST00000643479.1:n.1546G>T
|
|
|
ENST00000643516.1:c.869G>T
|
|
|
ENST00000644218.1:c.1171G>T
|
ENSP00000493574.1:p.Ala391Ser
|
|
ENST00000644683.1:c.*813G>T
|
ENSP00000494085.1:n.*813G>T
|
|
ENST00000644810.1:c.1081G>T
|
ENSP00000495895.1:p.Ala361Ser
|
|
ENST00000644831.1:n.1536G>T
|
|
|
ENST00000644933.1:c.*226G>T
|
ENSP00000496133.1:n.*226G>T
|
|
ENST00000645285.1:c.*226G>T
|
ENSP00000495058.1:n.*226G>T
|
|
ENST00000645331.1:n.2565G>T
|
|
|
ENST00000645620.1:c.631G>T
|
ENSP00000493657.1:p.Ala211Ser
|
|
ENST00000646691.1:n.1247G>T
|
|
|
ENST00000646777.1:n.1693G>T
|
|
|
ENST00000647016.1:n.1840G>T
|
|
|
ENST00000647152.1:c.631G>T
|
ENSP00000495893.1:p.Ala211Ser
|
|
ENST00000647209.1:c.*1229G>T
|
ENSP00000495558.1:n.*1229G>T
|
|
ENST00000647346.1:n.2380G>T
|
|
|
ENST00000299427.10:c.1360G>T
|
ENSP00000299427.6:p.Ala454Ser
|
|
ENST00000524611.1:n.238G>T
|
|
|
ENST00000532191.1:n.413G>T
|
|
|
ENST00000533371.5:c.631G>T
|
ENSP00000437066.1:p.Ala211Ser
|
|
ENST00000611494.4:c.1360G>T
|
ENSP00000484546.1:p.Ala454Ser
|
|
NM_000391.3:c.1360G>T
|
NP_000382.3:p.Ala454Ser
|
|
NM_000391.4:c.1360G>T
MANE Select
|
NP_000382.3:p.Ala454Ser
|
|