ENST00000236671.7:c.982C>A
MANE Select
|
ENSP00000236671.2:p.Pro328Thr
|
|
ENST00000367196.4:c.877C>A
|
ENSP00000356164.4:p.Pro293Thr
|
|
ENST00000427721.3:c.407C>A
|
|
|
ENST00000429746.2:c.877C>A
|
ENSP00000402586.2:p.Pro293Thr
|
|
ENST00000433655.6:c.*148C>A
|
ENSP00000404902.1:n.*148C>A
|
|
ENST00000438213.6:c.1099C>A
|
ENSP00000415036.2:p.Pro367Thr
|
|
ENST00000497544.3:n.690C>A
|
|
|
ENST00000636397.1:c.982C>A
|
ENSP00000489910.1:p.Pro328Thr
|
|
ENST00000636571.1:c.961C>A
|
ENSP00000490770.1:p.Pro321Thr
|
|
ENST00000636615.1:c.982C>A
|
ENSP00000490014.1:p.Pro328Thr
|
|
ENST00000636843.1:c.976C>A
|
ENSP00000490897.1:p.Pro326Thr
|
|
ENST00000637158.1:n.580C>A
|
|
|
ENST00000637381.2:n.3410C>A
|
|
|
ENST00000637387.1:c.973-12C>A
|
ENSP00000490598.1:n.973-12C>A
|
|
ENST00000637815.2:c.964C>A
|
ENSP00000490344.1:p.Pro322Thr
|
|
ENST00000637915.1:c.982C>A
|
ENSP00000490471.1:p.Pro328Thr
|
|
ENST00000637937.1:n.290C>A
|
|
|
ENST00000678991.1:c.*843C>A
|
ENSP00000503019.1:n.*843C>A
|
|
ENST00000236671.6:c.982C>A
|
ENSP00000236671.2:p.Pro328Thr
|
|
ENST00000427721.2:c.382C>A
|
ENSP00000415840.2:p.Pro128Thr
|
|
ENST00000429746.1:c.313C>A
|
ENSP00000402586.1:p.Pro105Thr
|
|
ENST00000433655.5:c.*148C>A
|
ENSP00000404902.1:n.*148C>A
|
|
ENST00000497544.1:n.690C>A
|
|
|
NM_001909.4:c.982C>A
|
NP_001900.1:p.Pro328Thr
|
|
NM_001909.5:c.982C>A
MANE Select
|
NP_001900.1:p.Pro328Thr
|
|