ENST00000005226.12:c.2270G>A
MANE Select
|
ENSP00000005226.7:p.Arg757His
|
|
ENST00000318024.9:c.1370G>A
MANE Plus Clinical
|
ENSP00000317018.4:p.Arg457His
|
|
ENST00000005226.11:c.2270G>A
|
ENSP00000005226.7:p.Arg757His
|
|
ENST00000318024.8:c.1370G>A
|
ENSP00000317018.4:p.Arg457His
|
|
ENST00000526313.5:c.*84G>A
|
ENSP00000432236.1:n.*84G>A
|
|
ENST00000527020.5:c.1313G>A
|
ENSP00000436934.1:p.Arg438His
|
|
ENST00000527720.5:c.1277G>A
|
ENSP00000432944.1:p.Arg426His
|
|
ENST00000529563.5:n.254G>A
|
|
|
ENST00000534556.1:n.155G>A
|
|
|
NM_001297764.1:c.1313G>A
|
NP_001284693.1:p.Arg438His
|
|
NM_005709.3:c.1370G>A
|
NP_005700.2:p.Arg457His
|
|
NM_153676.3:c.2270G>A
|
NP_710142.1:p.Arg757His
|
|
NR_123738.1:n.1405G>A
|
|
|
XM_011519831.1:c.2294G>A
|
XP_011518133.1:p.Arg765His
|
|
XM_011519832.1:c.1523G>A
|
XP_011518134.1:p.Arg508His
|
|
XM_011519833.1:c.1420G>A
|
XP_011518135.1:p.Ala474Thr
|
|
XR_930841.1:n.1741G>A
|
|
|
XR_930842.1:n.1682G>A
|
|
|
XM_011519832.3:c.1523G>A
|
XP_011518134.1:p.Arg508His
|
|
XM_017017075.1:c.2270G>A
|
XP_016872564.1:p.Arg757His
|
|
XR_001747717.2:n.1529G>A
|
|
|
NM_153676.4:c.2270G>A
MANE Select
|
NP_710142.1:p.Arg757His
|
|
NM_001297764.2:c.1313G>A
|
NP_001284693.1:p.Arg438His
|
|
NM_005709.4:c.1370G>A
MANE Plus Clinical
|
NP_005700.2:p.Arg457His
|
|
NR_123738.2:n.1405G>A
|
|
|