|
NM_001982.4:c.2564T>C
MANE Select
|
NP_001973.2:p.Val855Ala
|
|
ENST00000267101.8:c.2564T>C
MANE Select
|
ENSP00000267101.4:p.Val855Ala
|
|
NM_001982.3:c.2564T>C
|
NP_001973.2:p.Val855Ala
|
|
ENST00000267101.7:c.2564T>C
|
ENSP00000267101.3:p.Val855Ala
|
|
ENST00000415288.6:c.2387T>C
|
ENSP00000408340.2:p.Val796Ala
|
|
ENST00000548709.1:n.201T>C
|
|
|
ENST00000550070.6:c.538-612T>C
|
ENSP00000448946.2:n.538-612T>C
|
|
ENST00000551085.5:c.2564T>C
|
ENSP00000448483.1:p.Val855Ala
|
|
ENST00000551242.5:c.989-2294T>C
|
ENSP00000447510.1:n.989-2294T>C
|
|
ENST00000553131.5:c.287T>C
|
ENSP00000449129.1:p.Val96Ala
|
|
ENST00000682431.1:n.4050T>C
|
|
|
ENST00000682512.1:n.163T>C
|
|
|
ENST00000683018.1:c.2387T>C
|
ENSP00000506822.1:p.Val796Ala
|
|
ENST00000683059.1:c.2387T>C
|
ENSP00000507402.1:p.Val796Ala
|
|
ENST00000683142.1:n.244T>C
|
|
|
ENST00000683164.1:c.2387T>C
|
ENSP00000508051.1:p.Val796Ala
|
|
ENST00000683653.1:n.3297T>C
|
|
|
ENST00000684500.1:n.3605T>C
|
|
|
ENST00000684766.1:n.1361T>C
|
|
