|
ENST00000267868.8:c.877G>A
MANE Select
|
ENSP00000267868.3:p.Ala293Thr
|
|
|
ENST00000532743.6:c.877G>A
|
ENSP00000433924.2:p.Ala293Thr
|
|
|
ENST00000645673.2:c.880G>A
|
ENSP00000493712.2:p.Ala294Thr
|
|
|
ENST00000267868.7:c.877G>A
|
ENSP00000267868.3:p.Ala293Thr
|
|
|
ENST00000382643.7:c.880G>A
|
ENSP00000372088.3:p.Ala294Thr
|
|
|
ENST00000423169.6:c.774+321G>A
|
ENSP00000406602.2:n.774+321G>A
|
|
|
ENST00000525066.5:c.*326G>A
|
ENSP00000431864.1:n.*326G>A
|
|
|
ENST00000532743.5:c.880G>A
|
ENSP00000433924.1:p.Ala294Thr
|
|
|
ENST00000557850.5:c.586G>A
|
ENSP00000454176.1:p.Ala196Thr
|
|
|
NM_001164269.1:c.880G>A
|
NP_001157741.1:p.Ala294Thr
|
|
|
NM_001164270.1:c.774+321G>A
|
NP_001157742.1:n.774+321G>A
|
|
|
NM_002875.4:c.877G>A
|
NP_002866.2:p.Ala293Thr
|
|
|
NM_133487.3:c.880G>A
|
NP_597994.3:p.Ala294Thr
|
|
|
XM_006720626.2:c.877G>A
|
XP_006720689.1:p.Ala293Thr
|
|
|
XM_011521857.1:c.877G>A
|
XP_011520159.1:p.Ala293Thr
|
|
|
XM_011521858.1:c.877G>A
|
XP_011520160.1:p.Ala293Thr
|
|
|
XM_011521859.1:c.877G>A
|
XP_011520161.1:p.Ala293Thr
|
|
|
XM_011521860.1:c.877G>A
|
XP_011520162.1:p.Ala293Thr
|
|
|
XM_011521861.1:c.774+321G>A
|
XP_011520163.1:n.774+321G>A
|
|
|
XM_011521862.1:c.505G>A
|
XP_011520164.1:p.Ala169Thr
|
|
|
XM_006720626.3:c.877G>A
|
XP_006720689.1:p.Ala293Thr
|
|
|
XM_011521857.2:c.877G>A
|
XP_011520159.1:p.Ala293Thr
|
|
|
XM_011521858.2:c.877G>A
|
XP_011520160.1:p.Ala293Thr
|
|
|
XM_011521859.2:c.877G>A
|
XP_011520161.1:p.Ala293Thr
|
|
|
XM_011521860.2:c.877G>A
|
XP_011520162.1:p.Ala293Thr
|
|
|
XM_011521861.2:c.774+321G>A
|
XP_011520163.1:n.774+321G>A
|
|
|
XM_011521862.3:c.505G>A
|
XP_011520164.1:p.Ala169Thr
|
|
|
NM_001164269.2:c.880G>A
|
NP_001157741.1:p.Ala294Thr
|
|
|
NM_001164270.2:c.774+321G>A
|
NP_001157742.1:n.774+321G>A
|
|
|
NM_002875.5:c.877G>A
MANE Select
|
NP_002866.2:p.Ala293Thr
|
|
|
NM_133487.4:c.880G>A
|
NP_597994.3:p.Ala294Thr
|
|
