ENST00000682424.1:c.1549G>A
|
ENSP00000507321.1:p.Ala517Thr
|
|
ENST00000299427.12:c.1663G>A
MANE Select
|
ENSP00000299427.6:p.Ala555Thr
|
|
ENST00000524611.2:n.702G>A
|
|
|
ENST00000533371.6:c.934G>A
|
ENSP00000437066.1:p.Ala312Thr
|
|
ENST00000642892.1:c.934G>A
|
ENSP00000494165.1:p.Ala312Thr
|
|
ENST00000643342.1:c.736G>A
|
|
|
ENST00000643439.1:c.*1403G>A
|
ENSP00000495849.1:n.*1403G>A
|
|
ENST00000643479.1:n.1849G>A
|
|
|
ENST00000643516.1:c.1172G>A
|
|
|
ENST00000644218.1:c.1474G>A
|
ENSP00000493574.1:p.Ala492Thr
|
|
ENST00000644683.1:c.*1116G>A
|
ENSP00000494085.1:n.*1116G>A
|
|
ENST00000644810.1:c.1384G>A
|
ENSP00000495895.1:p.Ala462Thr
|
|
ENST00000644831.1:n.1839G>A
|
|
|
ENST00000644933.1:c.*529G>A
|
ENSP00000496133.1:n.*529G>A
|
|
ENST00000645285.1:c.*529G>A
|
ENSP00000495058.1:n.*529G>A
|
|
ENST00000645331.1:n.2868G>A
|
|
|
ENST00000645620.1:c.934G>A
|
ENSP00000493657.1:p.Ala312Thr
|
|
ENST00000646691.1:n.1550G>A
|
|
|
ENST00000646777.1:n.1996G>A
|
|
|
ENST00000647016.1:n.2143G>A
|
|
|
ENST00000647152.1:c.934G>A
|
ENSP00000495893.1:p.Ala312Thr
|
|
ENST00000647209.1:c.*1532G>A
|
ENSP00000495558.1:n.*1532G>A
|
|
ENST00000647346.1:n.2683G>A
|
|
|
ENST00000299427.10:c.1663G>A
|
ENSP00000299427.6:p.Ala555Thr
|
|
ENST00000533371.5:c.934G>A
|
ENSP00000437066.1:p.Ala312Thr
|
|
ENST00000611494.4:c.1662G>A
|
ENSP00000484546.1:p.Gln554=
|
|
NM_000391.3:c.1663G>A
|
NP_000382.3:p.Ala555Thr
|
|
NM_000391.4:c.1663G>A
MANE Select
|
NP_000382.3:p.Ala555Thr
|
|