ENST00000236671.7:c.1015A>C
MANE Select
|
ENSP00000236671.2:p.Thr339Pro
|
|
ENST00000367196.4:c.910A>C
|
ENSP00000356164.4:p.Thr304Pro
|
|
ENST00000427721.3:c.440A>C
|
|
|
ENST00000429746.2:c.910A>C
|
ENSP00000402586.2:p.Thr304Pro
|
|
ENST00000433655.6:c.*181A>C
|
ENSP00000404902.1:n.*181A>C
|
|
ENST00000438213.6:c.1132A>C
|
ENSP00000415036.2:p.Thr378Pro
|
|
ENST00000497544.3:n.723A>C
|
|
|
ENST00000636397.1:c.1015A>C
|
ENSP00000489910.1:p.Thr339Pro
|
|
ENST00000636571.1:c.994A>C
|
ENSP00000490770.1:p.Thr332Pro
|
|
ENST00000636579.1:c.16A>C
|
ENSP00000490489.1:p.Thr6Pro
|
|
ENST00000636615.1:c.1015A>C
|
ENSP00000490014.1:p.Thr339Pro
|
|
ENST00000636843.1:c.1009A>C
|
ENSP00000490897.1:p.Thr337Pro
|
|
ENST00000637158.1:n.613A>C
|
|
|
ENST00000637381.2:n.3443A>C
|
|
|
ENST00000637387.1:c.994A>C
|
ENSP00000490598.1:p.Thr332Pro
|
|
ENST00000637815.2:c.997A>C
|
ENSP00000490344.1:p.Thr333Pro
|
|
ENST00000637915.1:c.1015A>C
|
ENSP00000490471.1:p.Thr339Pro
|
|
ENST00000637937.1:n.323A>C
|
|
|
ENST00000678991.1:c.*876A>C
|
ENSP00000503019.1:n.*876A>C
|
|
ENST00000236671.6:c.1015A>C
|
ENSP00000236671.2:p.Thr339Pro
|
|
ENST00000427721.2:c.415A>C
|
ENSP00000415840.2:p.Thr139Pro
|
|
ENST00000429746.1:c.346A>C
|
ENSP00000402586.1:p.Thr116Pro
|
|
ENST00000433655.5:c.*181A>C
|
ENSP00000404902.1:n.*181A>C
|
|
ENST00000497544.1:n.723A>C
|
|
|
NM_001909.4:c.1015A>C
|
NP_001900.1:p.Thr339Pro
|
|
NM_001909.5:c.1015A>C
MANE Select
|
NP_001900.1:p.Thr339Pro
|
|