ENST00000005226.12:c.2241G>T
MANE Select
|
ENSP00000005226.7:p.Gln747His
|
|
ENST00000318024.9:c.1341G>T
MANE Plus Clinical
|
ENSP00000317018.4:p.Gln447His
|
|
ENST00000005226.11:c.2241G>T
|
ENSP00000005226.7:p.Gln747His
|
|
ENST00000318024.8:c.1341G>T
|
ENSP00000317018.4:p.Gln447His
|
|
ENST00000526313.5:c.*55G>T
|
ENSP00000432236.1:n.*55G>T
|
|
ENST00000527020.5:c.1284G>T
|
ENSP00000436934.1:p.Gln428His
|
|
ENST00000527720.5:c.1248G>T
|
ENSP00000432944.1:p.Gln416His
|
|
ENST00000529563.5:n.225G>T
|
|
|
ENST00000534556.1:n.126G>T
|
|
|
NM_001297764.1:c.1284G>T
|
NP_001284693.1:p.Gln428His
|
|
NM_005709.3:c.1341G>T
|
NP_005700.2:p.Gln447His
|
|
NM_153676.3:c.2241G>T
|
NP_710142.1:p.Gln747His
|
|
NR_123738.1:n.1376G>T
|
|
|
XM_011519831.1:c.2265G>T
|
XP_011518133.1:p.Gln755His
|
|
XM_011519832.1:c.1494G>T
|
XP_011518134.1:p.Gln498His
|
|
XM_011519833.1:c.1391G>T
|
XP_011518135.1:p.Arg464Ile
|
|
XR_930841.1:n.1712G>T
|
|
|
XR_930842.1:n.1653G>T
|
|
|
XM_011519832.3:c.1494G>T
|
XP_011518134.1:p.Gln498His
|
|
XM_017017075.1:c.2241G>T
|
XP_016872564.1:p.Gln747His
|
|
XR_001747717.2:n.1500G>T
|
|
|
NM_153676.4:c.2241G>T
MANE Select
|
NP_710142.1:p.Gln747His
|
|
NM_001297764.2:c.1284G>T
|
NP_001284693.1:p.Gln428His
|
|
NM_005709.4:c.1341G>T
MANE Plus Clinical
|
NP_005700.2:p.Gln447His
|
|
NR_123738.2:n.1376G>T
|
|
|