|
ENST00000371068.11:c.1637A>C
MANE Select
|
ENSP00000360107.4:p.Glu546Ala
|
|
|
ENST00000480623.6:c.1637A>C
|
ENSP00000434498.2:p.Glu546Ala
|
|
|
ENST00000635760.1:c.1313A>C
|
ENSP00000489765.1:p.Glu438Ala
|
|
|
ENST00000635812.1:c.*938A>C
|
ENSP00000490859.1:n.*938A>C
|
|
|
ENST00000635866.1:c.*1506A>C
|
ENSP00000489866.1:n.*1506A>C
|
|
|
ENST00000635911.1:n.3155A>C
|
|
|
|
ENST00000635984.1:c.1313A>C
|
ENSP00000489921.1:p.Glu438Ala
|
|
|
ENST00000635996.1:c.1637A>C
|
ENSP00000490256.1:p.Glu546Ala
|
|
|
ENST00000636107.1:c.1637A>C
|
ENSP00000489680.1:p.Glu546Ala
|
|
|
ENST00000636311.1:n.1531A>C
|
|
|
|
ENST00000636343.1:c.1303A>C
|
|
|
|
ENST00000636379.1:c.1349A>C
|
ENSP00000490622.1:p.Glu450Ala
|
|
|
ENST00000636398.1:c.1337A>C
|
ENSP00000489654.1:n.1337A>C
|
|
|
ENST00000636489.1:c.1580A>C
|
ENSP00000489998.1:p.Glu527Ala
|
|
|
ENST00000636616.1:n.1198A>C
|
|
|
|
ENST00000636702.1:c.1607A>C
|
ENSP00000489623.1:p.Glu536Ala
|
|
|
ENST00000636954.1:c.1580A>C
|
ENSP00000489966.1:p.Glu527Ala
|
|
|
ENST00000637089.1:c.1637A>C
|
ENSP00000489854.1:p.Glu546Ala
|
|
|
ENST00000637121.1:n.1439A>C
|
|
|
|
ENST00000637263.1:c.1637A>C
|
ENSP00000489700.1:p.Glu546Ala
|
|
|
ENST00000637340.1:n.3562A>C
|
|
|
|
ENST00000637353.1:c.1637A>C
|
ENSP00000490441.1:p.Glu546Ala
|
|
|
ENST00000637602.1:c.*1338A>C
|
ENSP00000490074.1:n.*1338A>C
|
|
|
ENST00000637849.1:n.1701A>C
|
|
|
|
ENST00000637892.1:n.1841A>C
|
|
|
|
ENST00000371068.9:c.1637A>C
|
ENSP00000360107.4:p.Glu546Ala
|
|
|
ENST00000480623.5:c.*2057A>C
|
ENSP00000434498.1:n.*2057A>C
|
|
|
ENST00000538167.2:c.1580A>C
|
ENSP00000444521.1:p.Glu527Ala
|
|
|
NM_001172420.1:c.1580A>C
|
NP_001165891.1:p.Glu527Ala
|
|
|
NM_018100.3:c.1637A>C
|
NP_060570.2:p.Glu546Ala
|
|
|
NR_033327.1:n.3109A>C
|
|
|
|
NM_018100.4:c.1637A>C
MANE Select
|
NP_060570.2:p.Glu546Ala
|
|
|
NM_001172420.2:c.1580A>C
|
NP_001165891.1:p.Glu527Ala
|
|
|
NR_033327.2:n.2963A>C
|
|
|
