ENST00000682424.1:c.1559A>C
|
ENSP00000507321.1:p.Lys520Thr
|
|
ENST00000299427.12:c.1673A>C
MANE Select
|
ENSP00000299427.6:p.Lys558Thr
|
|
ENST00000524611.2:n.712A>C
|
|
|
ENST00000533371.6:c.944A>C
|
ENSP00000437066.1:p.Lys315Thr
|
|
ENST00000642892.1:c.944A>C
|
ENSP00000494165.1:p.Lys315Thr
|
|
ENST00000643342.1:c.746A>C
|
|
|
ENST00000643439.1:c.*1413A>C
|
ENSP00000495849.1:n.*1413A>C
|
|
ENST00000643479.1:n.1859A>C
|
|
|
ENST00000643516.1:c.1182A>C
|
|
|
ENST00000644218.1:c.1484A>C
|
ENSP00000493574.1:p.Lys495Thr
|
|
ENST00000644683.1:c.*1126A>C
|
ENSP00000494085.1:n.*1126A>C
|
|
ENST00000644810.1:c.1394A>C
|
ENSP00000495895.1:p.Lys465Thr
|
|
ENST00000644831.1:n.1849A>C
|
|
|
ENST00000644933.1:c.*539A>C
|
ENSP00000496133.1:n.*539A>C
|
|
ENST00000645285.1:c.*539A>C
|
ENSP00000495058.1:n.*539A>C
|
|
ENST00000645331.1:n.2878A>C
|
|
|
ENST00000645620.1:c.944A>C
|
ENSP00000493657.1:p.Lys315Thr
|
|
ENST00000646691.1:n.1560A>C
|
|
|
ENST00000646777.1:n.2006A>C
|
|
|
ENST00000647016.1:n.2153A>C
|
|
|
ENST00000647152.1:c.944A>C
|
ENSP00000495893.1:p.Lys315Thr
|
|
ENST00000647209.1:c.*1542A>C
|
ENSP00000495558.1:n.*1542A>C
|
|
ENST00000647346.1:n.2693A>C
|
|
|
ENST00000299427.10:c.1673A>C
|
ENSP00000299427.6:p.Lys558Thr
|
|
ENST00000533371.5:c.944A>C
|
ENSP00000437066.1:p.Lys315Thr
|
|
ENST00000611494.4:c.*1A>C
|
ENSP00000484546.1:n.*1A>C
|
|
NM_000391.3:c.1673A>C
|
NP_000382.3:p.Lys558Thr
|
|
NM_000391.4:c.1673A>C
MANE Select
|
NP_000382.3:p.Lys558Thr
|
|