ENST00000236671.7:c.633G>T
MANE Select
|
ENSP00000236671.2:p.Val211=
|
|
ENST00000367196.4:c.528G>T
|
ENSP00000356164.4:p.Val176=
|
|
ENST00000427721.3:c.58G>T
|
|
|
ENST00000429746.2:c.528G>T
|
ENSP00000402586.2:p.Val176=
|
|
ENST00000433655.6:c.633G>T
|
ENSP00000404902.1:p.Val211=
|
|
ENST00000438213.6:c.633G>T
|
ENSP00000415036.2:p.Val211=
|
|
ENST00000636397.1:c.633G>T
|
ENSP00000489910.1:p.Val211=
|
|
ENST00000636571.1:c.612G>T
|
ENSP00000490770.1:p.Val204=
|
|
ENST00000636615.1:c.633G>T
|
ENSP00000490014.1:p.Val211=
|
|
ENST00000636843.1:c.627G>T
|
ENSP00000490897.1:p.Val209=
|
|
ENST00000637158.1:n.231G>T
|
|
|
ENST00000637381.2:n.3061G>T
|
|
|
ENST00000637387.1:c.633G>T
|
ENSP00000490598.1:p.Val211=
|
|
ENST00000637815.2:c.633G>T
|
ENSP00000490344.1:p.Val211=
|
|
ENST00000637915.1:c.633G>T
|
ENSP00000490471.1:p.Val211=
|
|
ENST00000677300.1:n.1028G>T
|
|
|
ENST00000678991.1:c.*494G>T
|
ENSP00000503019.1:n.*494G>T
|
|
ENST00000236671.6:c.633G>T
|
ENSP00000236671.2:p.Val211=
|
|
ENST00000367196.3:c.528G>T
|
ENSP00000356164.3:p.Val176=
|
|
ENST00000427721.2:c.33G>T
|
ENSP00000415840.2:p.Val11=
|
|
ENST00000433655.5:c.633G>T
|
ENSP00000404902.1:p.Val211=
|
|
ENST00000438213.5:c.588G>T
|
ENSP00000415036.1:p.Val196=
|
|
NM_001909.4:c.633G>T
|
NP_001900.1:p.Val211=
|
|
NM_001909.5:c.633G>T
MANE Select
|
NP_001900.1:p.Val211=
|
|