ENST00000236671.7:c.1017A>T
MANE Select
|
ENSP00000236671.2:p.Thr339=
|
|
ENST00000367196.4:c.912A>T
|
ENSP00000356164.4:p.Thr304=
|
|
ENST00000427721.3:c.442A>T
|
|
|
ENST00000429746.2:c.912A>T
|
ENSP00000402586.2:p.Thr304=
|
|
ENST00000433655.6:c.*183A>T
|
ENSP00000404902.1:n.*183A>T
|
|
ENST00000438213.6:c.1134A>T
|
ENSP00000415036.2:p.Thr378=
|
|
ENST00000497544.3:n.725A>T
|
|
|
ENST00000636397.1:c.1017A>T
|
ENSP00000489910.1:p.Thr339=
|
|
ENST00000636571.1:c.996A>T
|
ENSP00000490770.1:p.Thr332=
|
|
ENST00000636579.1:c.18A>T
|
ENSP00000490489.1:p.Thr6=
|
|
ENST00000636615.1:c.1017A>T
|
ENSP00000490014.1:p.Thr339=
|
|
ENST00000636843.1:c.1011A>T
|
ENSP00000490897.1:p.Thr337=
|
|
ENST00000637158.1:n.615A>T
|
|
|
ENST00000637381.2:n.3445A>T
|
|
|
ENST00000637387.1:c.996A>T
|
ENSP00000490598.1:p.Thr332=
|
|
ENST00000637815.2:c.999A>T
|
ENSP00000490344.1:p.Thr333=
|
|
ENST00000637915.1:c.1017A>T
|
ENSP00000490471.1:p.Thr339=
|
|
ENST00000637937.1:n.325A>T
|
|
|
ENST00000678991.1:c.*878A>T
|
ENSP00000503019.1:n.*878A>T
|
|
ENST00000236671.6:c.1017A>T
|
ENSP00000236671.2:p.Thr339=
|
|
ENST00000427721.2:c.417A>T
|
ENSP00000415840.2:p.Thr139=
|
|
ENST00000429746.1:c.348A>T
|
ENSP00000402586.1:p.Thr116=
|
|
ENST00000433655.5:c.*183A>T
|
ENSP00000404902.1:n.*183A>T
|
|
ENST00000497544.1:n.725A>T
|
|
|
NM_001909.4:c.1017A>T
|
NP_001900.1:p.Thr339=
|
|
NM_001909.5:c.1017A>T
MANE Select
|
NP_001900.1:p.Thr339=
|
|