ENST00000236671.7:c.998C>A
MANE Select
|
ENSP00000236671.2:p.Ser333Tyr
|
|
ENST00000367196.4:c.893C>A
|
ENSP00000356164.4:p.Ser298Tyr
|
|
ENST00000427721.3:c.423C>A
|
|
|
ENST00000429746.2:c.893C>A
|
ENSP00000402586.2:p.Ser298Tyr
|
|
ENST00000433655.6:c.*164C>A
|
ENSP00000404902.1:n.*164C>A
|
|
ENST00000438213.6:c.1115C>A
|
ENSP00000415036.2:p.Ser372Tyr
|
|
ENST00000497544.3:n.706C>A
|
|
|
ENST00000636397.1:c.998C>A
|
ENSP00000489910.1:p.Ser333Tyr
|
|
ENST00000636571.1:c.977C>A
|
ENSP00000490770.1:p.Ser326Tyr
|
|
ENST00000636615.1:c.998C>A
|
ENSP00000490014.1:p.Ser333Tyr
|
|
ENST00000636843.1:c.992C>A
|
ENSP00000490897.1:p.Ser331Tyr
|
|
ENST00000637158.1:n.596C>A
|
|
|
ENST00000637381.2:n.3426C>A
|
|
|
ENST00000637387.1:c.977C>A
|
ENSP00000490598.1:p.Ser326Tyr
|
|
ENST00000637815.2:c.980C>A
|
ENSP00000490344.1:p.Ser327Tyr
|
|
ENST00000637915.1:c.998C>A
|
ENSP00000490471.1:p.Ser333Tyr
|
|
ENST00000637937.1:n.306C>A
|
|
|
ENST00000678991.1:c.*859C>A
|
ENSP00000503019.1:n.*859C>A
|
|
ENST00000236671.6:c.998C>A
|
ENSP00000236671.2:p.Ser333Tyr
|
|
ENST00000427721.2:c.398C>A
|
ENSP00000415840.2:p.Ser133Tyr
|
|
ENST00000429746.1:c.329C>A
|
ENSP00000402586.1:p.Ser110Tyr
|
|
ENST00000433655.5:c.*164C>A
|
ENSP00000404902.1:n.*164C>A
|
|
ENST00000497544.1:n.706C>A
|
|
|
NM_001909.4:c.998C>A
|
NP_001900.1:p.Ser333Tyr
|
|
NM_001909.5:c.998C>A
MANE Select
|
NP_001900.1:p.Ser333Tyr
|
|