ENST00000682424.1:c.1159G>T
|
ENSP00000507321.1:p.Ala387Ser
|
|
ENST00000299427.12:c.1273G>T
MANE Select
|
ENSP00000299427.6:p.Ala425Ser
|
|
ENST00000436873.7:c.510G>T
|
|
|
ENST00000524611.2:n.133G>T
|
|
|
ENST00000524924.2:n.393G>T
|
|
|
ENST00000533371.6:c.544G>T
|
ENSP00000437066.1:p.Ala182Ser
|
|
ENST00000642892.1:c.544G>T
|
ENSP00000494165.1:p.Ala182Ser
|
|
ENST00000643342.1:c.346G>T
|
|
|
ENST00000643439.1:c.*1013G>T
|
ENSP00000495849.1:n.*1013G>T
|
|
ENST00000643479.1:n.1459G>T
|
|
|
ENST00000643516.1:c.782G>T
|
|
|
ENST00000644218.1:c.1084G>T
|
ENSP00000493574.1:p.Ala362Ser
|
|
ENST00000644683.1:c.*726G>T
|
ENSP00000494085.1:n.*726G>T
|
|
ENST00000644810.1:c.994G>T
|
ENSP00000495895.1:p.Ala332Ser
|
|
ENST00000644831.1:n.1449G>T
|
|
|
ENST00000644933.1:c.*139G>T
|
ENSP00000496133.1:n.*139G>T
|
|
ENST00000645285.1:c.*139G>T
|
ENSP00000495058.1:n.*139G>T
|
|
ENST00000645331.1:n.2478G>T
|
|
|
ENST00000645620.1:c.544G>T
|
ENSP00000493657.1:p.Ala182Ser
|
|
ENST00000646691.1:n.1160G>T
|
|
|
ENST00000646777.1:n.1606G>T
|
|
|
ENST00000647016.1:n.1753G>T
|
|
|
ENST00000647152.1:c.544G>T
|
ENSP00000495893.1:p.Ala182Ser
|
|
ENST00000647209.1:c.*1142G>T
|
ENSP00000495558.1:n.*1142G>T
|
|
ENST00000647346.1:n.2293G>T
|
|
|
ENST00000299427.10:c.1273G>T
|
ENSP00000299427.6:p.Ala425Ser
|
|
ENST00000524611.1:n.151G>T
|
|
|
ENST00000524924.1:n.228G>T
|
|
|
ENST00000532191.1:n.326G>T
|
|
|
ENST00000533371.5:c.544G>T
|
ENSP00000437066.1:p.Ala182Ser
|
|
ENST00000611494.4:c.1273G>T
|
ENSP00000484546.1:p.Ala425Ser
|
|
NM_000391.3:c.1273G>T
|
NP_000382.3:p.Ala425Ser
|
|
NM_000391.4:c.1273G>T
MANE Select
|
NP_000382.3:p.Ala425Ser
|
|