|
ENST00000371068.11:c.1634C>T
MANE Select
|
ENSP00000360107.4:p.Ala545Val
|
|
|
ENST00000480623.6:c.1634C>T
|
ENSP00000434498.2:p.Ala545Val
|
|
|
ENST00000635760.1:c.1310C>T
|
ENSP00000489765.1:p.Ala437Val
|
|
|
ENST00000635812.1:c.*935C>T
|
ENSP00000490859.1:n.*935C>T
|
|
|
ENST00000635866.1:c.*1503C>T
|
ENSP00000489866.1:n.*1503C>T
|
|
|
ENST00000635911.1:n.3152C>T
|
|
|
|
ENST00000635984.1:c.1310C>T
|
ENSP00000489921.1:p.Ala437Val
|
|
|
ENST00000635996.1:c.1634C>T
|
ENSP00000490256.1:p.Ala545Val
|
|
|
ENST00000636107.1:c.1634C>T
|
ENSP00000489680.1:p.Ala545Val
|
|
|
ENST00000636311.1:n.1528C>T
|
|
|
|
ENST00000636343.1:c.1300C>T
|
|
|
|
ENST00000636379.1:c.1346C>T
|
ENSP00000490622.1:p.Ala449Val
|
|
|
ENST00000636398.1:c.1334C>T
|
ENSP00000489654.1:n.1334C>T
|
|
|
ENST00000636489.1:c.1577C>T
|
ENSP00000489998.1:p.Ala526Val
|
|
|
ENST00000636616.1:n.1195C>T
|
|
|
|
ENST00000636702.1:c.1604C>T
|
ENSP00000489623.1:p.Ala535Val
|
|
|
ENST00000636954.1:c.1577C>T
|
ENSP00000489966.1:p.Ala526Val
|
|
|
ENST00000637089.1:c.1634C>T
|
ENSP00000489854.1:p.Ala545Val
|
|
|
ENST00000637121.1:n.1436C>T
|
|
|
|
ENST00000637263.1:c.1634C>T
|
ENSP00000489700.1:p.Ala545Val
|
|
|
ENST00000637340.1:n.3559C>T
|
|
|
|
ENST00000637353.1:c.1634C>T
|
ENSP00000490441.1:p.Ala545Val
|
|
|
ENST00000637602.1:c.*1335C>T
|
ENSP00000490074.1:n.*1335C>T
|
|
|
ENST00000637849.1:n.1698C>T
|
|
|
|
ENST00000637892.1:n.1838C>T
|
|
|
|
ENST00000371068.9:c.1634C>T
|
ENSP00000360107.4:p.Ala545Val
|
|
|
ENST00000480623.5:c.*2054C>T
|
ENSP00000434498.1:n.*2054C>T
|
|
|
ENST00000538167.2:c.1577C>T
|
ENSP00000444521.1:p.Ala526Val
|
|
|
NM_001172420.1:c.1577C>T
|
NP_001165891.1:p.Ala526Val
|
|
|
NM_018100.3:c.1634C>T
|
NP_060570.2:p.Ala545Val
|
|
|
NR_033327.1:n.3106C>T
|
|
|
|
NM_018100.4:c.1634C>T
MANE Select
|
NP_060570.2:p.Ala545Val
|
|
|
NM_001172420.2:c.1577C>T
|
NP_001165891.1:p.Ala526Val
|
|
|
NR_033327.2:n.2960C>T
|
|
|
