ENST00000236671.7:c.1075T>A
MANE Select
|
ENSP00000236671.2:p.Ser359Thr
|
|
ENST00000367196.4:c.970T>A
|
ENSP00000356164.4:p.Ser324Thr
|
|
ENST00000427721.3:c.500T>A
|
|
|
ENST00000429746.2:c.970T>A
|
ENSP00000402586.2:p.Ser324Thr
|
|
ENST00000433655.6:c.*241T>A
|
ENSP00000404902.1:n.*241T>A
|
|
ENST00000438213.6:c.1192T>A
|
ENSP00000415036.2:p.Ser398Thr
|
|
ENST00000497544.3:n.783T>A
|
|
|
ENST00000636397.1:c.1071+136T>A
|
ENSP00000489910.1:n.1071+136T>A
|
|
ENST00000636571.1:c.1054T>A
|
ENSP00000490770.1:p.Ser352Thr
|
|
ENST00000636579.1:c.72+136T>A
|
ENSP00000490489.1:n.72+136T>A
|
|
ENST00000636615.1:c.1071+136T>A
|
ENSP00000490014.1:n.1071+136T>A
|
|
ENST00000636843.1:c.1069T>A
|
ENSP00000490897.1:p.Ser357Thr
|
|
ENST00000637158.1:n.673T>A
|
|
|
ENST00000637381.2:n.3503T>A
|
|
|
ENST00000637387.1:c.1054T>A
|
ENSP00000490598.1:p.Ser352Thr
|
|
ENST00000637815.2:c.1057T>A
|
ENSP00000490344.1:p.Ser353Thr
|
|
ENST00000637915.1:c.1072-6T>A
|
ENSP00000490471.1:n.1072-6T>A
|
|
ENST00000637937.1:n.383T>A
|
|
|
ENST00000678991.1:c.*936T>A
|
ENSP00000503019.1:n.*936T>A
|
|
ENST00000236671.6:c.1075T>A
|
ENSP00000236671.2:p.Ser359Thr
|
|
ENST00000427721.2:c.471+136T>A
|
ENSP00000415840.2:n.471+136T>A
|
|
ENST00000429746.1:c.406T>A
|
ENSP00000402586.1:p.Ser136Thr
|
|
ENST00000433655.5:c.*241T>A
|
ENSP00000404902.1:n.*241T>A
|
|
NM_001909.4:c.1075T>A
|
NP_001900.1:p.Ser359Thr
|
|
NM_001909.5:c.1075T>A
MANE Select
|
NP_001900.1:p.Ser359Thr
|
|