ENST00000236671.7:c.955C>A
MANE Select
|
ENSP00000236671.2:p.Pro319Thr
|
|
ENST00000367196.4:c.850C>A
|
ENSP00000356164.4:p.Pro284Thr
|
|
ENST00000427721.3:c.380C>A
|
|
|
ENST00000429746.2:c.850C>A
|
ENSP00000402586.2:p.Pro284Thr
|
|
ENST00000433655.6:c.*121C>A
|
ENSP00000404902.1:n.*121C>A
|
|
ENST00000438213.6:c.1072C>A
|
ENSP00000415036.2:p.Pro358Thr
|
|
ENST00000497544.3:n.571C>A
|
|
|
ENST00000636397.1:c.955C>A
|
ENSP00000489910.1:p.Pro319Thr
|
|
ENST00000636571.1:c.934C>A
|
ENSP00000490770.1:p.Pro312Thr
|
|
ENST00000636615.1:c.955C>A
|
ENSP00000490014.1:p.Pro319Thr
|
|
ENST00000636843.1:c.949C>A
|
ENSP00000490897.1:p.Pro317Thr
|
|
ENST00000637158.1:n.553C>A
|
|
|
ENST00000637381.2:n.3383C>A
|
|
|
ENST00000637387.1:c.955C>A
|
ENSP00000490598.1:p.Pro319Thr
|
|
ENST00000637815.2:c.937C>A
|
ENSP00000490344.1:p.Pro313Thr
|
|
ENST00000637915.1:c.955C>A
|
ENSP00000490471.1:p.Pro319Thr
|
|
ENST00000637937.1:n.263C>A
|
|
|
ENST00000678991.1:c.*816C>A
|
ENSP00000503019.1:n.*816C>A
|
|
ENST00000236671.6:c.955C>A
|
ENSP00000236671.2:p.Pro319Thr
|
|
ENST00000427721.2:c.355C>A
|
ENSP00000415840.2:p.Pro119Thr
|
|
ENST00000429746.1:c.286C>A
|
ENSP00000402586.1:p.Pro96Thr
|
|
ENST00000433655.5:c.*121C>A
|
ENSP00000404902.1:n.*121C>A
|
|
ENST00000497544.1:n.571C>A
|
|
|
NM_001909.4:c.955C>A
|
NP_001900.1:p.Pro319Thr
|
|
NM_001909.5:c.955C>A
MANE Select
|
NP_001900.1:p.Pro319Thr
|
|