ENST00000236671.7:c.1176C>T
MANE Select
|
ENSP00000236671.2:p.Arg392=
|
|
ENST00000367196.4:c.1071C>T
|
ENSP00000356164.4:p.Arg357=
|
|
ENST00000427721.3:c.601C>T
|
|
|
ENST00000429746.2:c.1071C>T
|
ENSP00000402586.2:p.Arg357=
|
|
ENST00000433655.6:c.*342C>T
|
ENSP00000404902.1:n.*342C>T
|
|
ENST00000438213.6:c.1293C>T
|
ENSP00000415036.2:p.Arg431=
|
|
ENST00000636397.1:c.1071+237C>T
|
ENSP00000489910.1:n.1071+237C>T
|
|
ENST00000636571.1:c.1155C>T
|
ENSP00000490770.1:p.Arg385=
|
|
ENST00000636579.1:c.72+237C>T
|
ENSP00000490489.1:n.72+237C>T
|
|
ENST00000636615.1:c.1071+237C>T
|
ENSP00000490014.1:n.1071+237C>T
|
|
ENST00000636843.1:c.1170C>T
|
ENSP00000490897.1:p.Arg390=
|
|
ENST00000637158.1:n.774C>T
|
|
|
ENST00000637381.2:n.3604C>T
|
|
|
ENST00000637387.1:c.1155C>T
|
ENSP00000490598.1:p.Arg385=
|
|
ENST00000637815.2:c.1158C>T
|
ENSP00000490344.1:p.Arg386=
|
|
ENST00000637915.1:c.1167C>T
|
ENSP00000490471.1:p.Arg389=
|
|
ENST00000637937.1:n.484C>T
|
|
|
ENST00000678991.1:c.*1037C>T
|
ENSP00000503019.1:n.*1037C>T
|
|
ENST00000236671.6:c.1176C>T
|
ENSP00000236671.2:p.Arg392=
|
|
ENST00000427721.2:c.471+237C>T
|
ENSP00000415840.2:n.471+237C>T
|
|
ENST00000429746.1:c.507C>T
|
ENSP00000402586.1:p.Arg169=
|
|
ENST00000433655.5:c.*342C>T
|
ENSP00000404902.1:n.*342C>T
|
|
NM_001909.4:c.1176C>T
|
NP_001900.1:p.Arg392=
|
|
NM_001909.5:c.1176C>T
MANE Select
|
NP_001900.1:p.Arg392=
|
|