ENST00000236671.7:c.1131A>T
MANE Select
|
ENSP00000236671.2:p.Pro377=
|
|
ENST00000367196.4:c.1026A>T
|
ENSP00000356164.4:p.Pro342=
|
|
ENST00000427721.3:c.556A>T
|
|
|
ENST00000429746.2:c.1026A>T
|
ENSP00000402586.2:p.Pro342=
|
|
ENST00000433655.6:c.*297A>T
|
ENSP00000404902.1:n.*297A>T
|
|
ENST00000438213.6:c.1248A>T
|
ENSP00000415036.2:p.Pro416=
|
|
ENST00000636397.1:c.1071+192A>T
|
ENSP00000489910.1:n.1071+192A>T
|
|
ENST00000636571.1:c.1110A>T
|
ENSP00000490770.1:p.Pro370=
|
|
ENST00000636579.1:c.72+192A>T
|
ENSP00000490489.1:n.72+192A>T
|
|
ENST00000636615.1:c.1071+192A>T
|
ENSP00000490014.1:n.1071+192A>T
|
|
ENST00000636843.1:c.1125A>T
|
ENSP00000490897.1:p.Pro375=
|
|
ENST00000637158.1:n.729A>T
|
|
|
ENST00000637381.2:n.3559A>T
|
|
|
ENST00000637387.1:c.1110A>T
|
ENSP00000490598.1:p.Pro370=
|
|
ENST00000637815.2:c.1113A>T
|
ENSP00000490344.1:p.Pro371=
|
|
ENST00000637915.1:c.1122A>T
|
ENSP00000490471.1:p.Pro374=
|
|
ENST00000637937.1:n.439A>T
|
|
|
ENST00000678991.1:c.*992A>T
|
ENSP00000503019.1:n.*992A>T
|
|
ENST00000236671.6:c.1131A>T
|
ENSP00000236671.2:p.Pro377=
|
|
ENST00000427721.2:c.471+192A>T
|
ENSP00000415840.2:n.471+192A>T
|
|
ENST00000429746.1:c.462A>T
|
ENSP00000402586.1:p.Pro154=
|
|
ENST00000433655.5:c.*297A>T
|
ENSP00000404902.1:n.*297A>T
|
|
NM_001909.4:c.1131A>T
|
NP_001900.1:p.Pro377=
|
|
NM_001909.5:c.1131A>T
MANE Select
|
NP_001900.1:p.Pro377=
|
|