ENST00000236671.7:c.1077G>C
MANE Select
|
ENSP00000236671.2:p.Ser359=
|
|
ENST00000367196.4:c.972G>C
|
ENSP00000356164.4:p.Ser324=
|
|
ENST00000427721.3:c.502G>C
|
|
|
ENST00000429746.2:c.972G>C
|
ENSP00000402586.2:p.Ser324=
|
|
ENST00000433655.6:c.*243G>C
|
ENSP00000404902.1:n.*243G>C
|
|
ENST00000438213.6:c.1194G>C
|
ENSP00000415036.2:p.Ser398=
|
|
ENST00000497544.3:n.785G>C
|
|
|
ENST00000636397.1:c.1071+138G>C
|
ENSP00000489910.1:n.1071+138G>C
|
|
ENST00000636571.1:c.1056G>C
|
ENSP00000490770.1:p.Ser352=
|
|
ENST00000636579.1:c.72+138G>C
|
ENSP00000490489.1:n.72+138G>C
|
|
ENST00000636615.1:c.1071+138G>C
|
ENSP00000490014.1:n.1071+138G>C
|
|
ENST00000636843.1:c.1071G>C
|
ENSP00000490897.1:p.Ser357=
|
|
ENST00000637158.1:n.675G>C
|
|
|
ENST00000637381.2:n.3505G>C
|
|
|
ENST00000637387.1:c.1056G>C
|
ENSP00000490598.1:p.Ser352=
|
|
ENST00000637815.2:c.1059G>C
|
ENSP00000490344.1:p.Ser353=
|
|
ENST00000637915.1:c.1072-4G>C
|
ENSP00000490471.1:n.1072-4G>C
|
|
ENST00000637937.1:n.385G>C
|
|
|
ENST00000678991.1:c.*938G>C
|
ENSP00000503019.1:n.*938G>C
|
|
ENST00000236671.6:c.1077G>C
|
ENSP00000236671.2:p.Ser359=
|
|
ENST00000427721.2:c.471+138G>C
|
ENSP00000415840.2:n.471+138G>C
|
|
ENST00000429746.1:c.408G>C
|
ENSP00000402586.1:p.Ser136=
|
|
ENST00000433655.5:c.*243G>C
|
ENSP00000404902.1:n.*243G>C
|
|
NM_001909.4:c.1077G>C
|
NP_001900.1:p.Ser359=
|
|
NM_001909.5:c.1077G>C
MANE Select
|
NP_001900.1:p.Ser359=
|
|