ENST00000350026.11:c.4764G=
|
ENSP00000055163.8:p.Gln1588=
|
|
ENST00000414678.8:c.4833G=
|
ENSP00000412835.3:p.Gln1611=
|
|
ENST00000637015.2:c.5052G=
|
ENSP00000489729.2:p.Gln1684=
|
|
ENST00000346085.10:c.4803G=
|
ENSP00000344546.5:p.Gln1601=
|
|
ENST00000350026.10:c.4515G=
|
ENSP00000055163.7:p.Gln1505=
|
|
ENST00000414678.7:c.3081G=
|
ENSP00000412835.2:p.Gln1027=
|
|
ENST00000635849.1:c.2244G=
|
ENSP00000490948.1:p.Gln748=
|
|
ENST00000635957.1:c.1875G=
|
ENSP00000490385.1:p.Gln625=
|
|
ENST00000636227.1:n.3386G=
|
|
|
ENST00000636254.1:n.843G=
|
|
|
ENST00000636930.2:c.4923G=
MANE Select
|
ENSP00000490491.2:p.Gln1641=
|
|
ENST00000636940.1:n.2920G=
|
|
|
ENST00000637015.1:c.2291G=
|
|
|
ENST00000637568.1:c.2205G=
|
|
|
ENST00000637741.1:n.1589G=
|
|
|
ENST00000637810.1:c.2265G=
|
ENSP00000489636.1:p.Gln755=
|
|
ENST00000637904.1:c.2424G=
|
ENSP00000490550.1:p.Gln808=
|
|
ENST00000647938.1:c.4554G=
|
ENSP00000498155.1:p.Gln1518=
|
|
ENST00000346085.9:c.4554G=
|
ENSP00000344546.4:p.Gln1518=
|
|
ENST00000350026.9:c.4515G=
|
ENSP00000055163.7:p.Gln1505=
|
|
ENST00000414678.6:c.3081G=
|
ENSP00000412835.2:p.Gln1027=
|
|
NM_017519.2:c.4515G=
|
NP_059989.2:p.Gln1505=
|
|
NM_020732.3:c.4554G=
|
NP_065783.3:p.Gln1518=
|
|
XM_005267069.3:c.4674G=
|
XP_005267126.2:p.Gln1558=
|
|
XM_011535984.1:c.3753G=
|
XP_011534286.1:p.Gln1251=
|
|
XM_011535985.1:c.3573G=
|
XP_011534287.1:p.Gln1191=
|
|
XM_011535986.1:c.3333G=
|
XP_011534288.1:p.Gln1111=
|
|
XM_011535987.1:c.2952G=
|
XP_011534289.1:p.Gln984=
|
|
XM_011535988.1:c.1815G=
|
XP_011534290.1:p.Gln605=
|
|
NM_001346813.1:c.4674G=
|
NP_001333742.1:p.Gln1558=
|
|
NM_001363725.1:c.2424G=
|
NP_001350654.1:p.Gln808=
|
|
XM_011535984.2:c.4884G=
|
XP_011534286.2:p.Gln1628=
|
|
XM_011535988.3:c.1815G=
|
XP_011534290.1:p.Gln605=
|
|
XM_017011103.2:c.4785G=
|
XP_016866592.1:p.Gln1595=
|
|
XM_017011104.1:c.4755G=
|
XP_016866593.1:p.Gln1585=
|
|
XM_017011105.2:c.4725G=
|
XP_016866594.1:p.Gln1575=
|
|
XM_017011106.2:c.4596G=
|
XP_016866595.1:p.Gln1532=
|
|
XM_017011107.2:c.4575G=
|
XP_016866596.1:p.Gln1525=
|
|
XR_002956289.1:n.4870G=
|
|
|
NM_001363725.2:c.2424G=
|
NP_001350654.1:p.Gln808=
|
|
NM_001371656.1:c.4803G=
|
NP_001358585.1:p.Gln1601=
|
|
NM_001374820.1:c.4803G=
|
NP_001361749.1:p.Gln1601=
|
|
NM_001374828.1:c.4923G=
MANE Select
|
NP_001361757.1:p.Gln1641=
|
|
NM_017519.3:c.4764G=
|
NP_059989.3:p.Gln1588=
|
|