ENST00000005226.12:c.2379T>A
MANE Select
|
ENSP00000005226.7:p.His793Gln
|
|
ENST00000318024.9:c.1479T>A
MANE Plus Clinical
|
ENSP00000317018.4:p.His493Gln
|
|
ENST00000005226.11:c.2379T>A
|
ENSP00000005226.7:p.His793Gln
|
|
ENST00000318024.8:c.1479T>A
|
ENSP00000317018.4:p.His493Gln
|
|
ENST00000526313.5:c.*193T>A
|
ENSP00000432236.1:n.*193T>A
|
|
ENST00000527020.5:c.1422T>A
|
ENSP00000436934.1:p.His474Gln
|
|
ENST00000527720.5:c.1386T>A
|
ENSP00000432944.1:p.His462Gln
|
|
ENST00000529563.5:n.363T>A
|
|
|
NM_001297764.1:c.1422T>A
|
NP_001284693.1:p.His474Gln
|
|
NM_005709.3:c.1479T>A
|
NP_005700.2:p.His493Gln
|
|
NM_153676.3:c.2379T>A
|
NP_710142.1:p.His793Gln
|
|
NR_123738.1:n.1514T>A
|
|
|
XM_011519831.1:c.2403T>A
|
XP_011518133.1:p.His801Gln
|
|
XM_011519832.1:c.1632T>A
|
XP_011518134.1:p.His544Gln
|
|
XM_011519833.1:c.*86T>A
|
XP_011518135.1:n.*86T>A
|
|
XR_930841.1:n.1850T>A
|
|
|
XR_930842.1:n.1791T>A
|
|
|
XM_011519832.3:c.1632T>A
|
XP_011518134.1:p.His544Gln
|
|
XM_017017075.1:c.2379T>A
|
XP_016872564.1:p.His793Gln
|
|
XR_001747717.2:n.1638T>A
|
|
|
NM_153676.4:c.2379T>A
MANE Select
|
NP_710142.1:p.His793Gln
|
|
NM_001297764.2:c.1422T>A
|
NP_001284693.1:p.His474Gln
|
|
NM_005709.4:c.1479T>A
MANE Plus Clinical
|
NP_005700.2:p.His493Gln
|
|
NR_123738.2:n.1514T>A
|
|
|