ENST00000236671.7:c.1239G>C
MANE Select
|
ENSP00000236671.2:p.Ter413Tyr
|
|
ENST00000367196.4:c.1134G>C
|
ENSP00000356164.4:p.Ter378Tyr
|
|
ENST00000427721.3:c.634+30G>C
|
|
|
ENST00000429746.2:c.1134G>C
|
ENSP00000402586.2:p.Ter378Tyr
|
|
ENST00000433655.6:c.*405G>C
|
ENSP00000404902.1:n.*405G>C
|
|
ENST00000438213.6:c.1356G>C
|
ENSP00000415036.2:p.Ter452Tyr
|
|
ENST00000636397.1:c.1071+300G>C
|
ENSP00000489910.1:n.1071+300G>C
|
|
ENST00000636571.1:c.1218G>C
|
ENSP00000490770.1:p.Ter406Tyr
|
|
ENST00000636579.1:c.72+300G>C
|
ENSP00000490489.1:n.72+300G>C
|
|
ENST00000636615.1:c.1071+300G>C
|
ENSP00000490014.1:n.1071+300G>C
|
|
ENST00000636843.1:c.1233G>C
|
ENSP00000490897.1:p.Ter411Tyr
|
|
ENST00000637158.1:n.837G>C
|
|
|
ENST00000637381.2:n.3667G>C
|
|
|
ENST00000637387.1:c.1218G>C
|
ENSP00000490598.1:p.Ter406Tyr
|
|
ENST00000637815.2:c.1221G>C
|
ENSP00000490344.1:p.Ter407Tyr
|
|
ENST00000637915.1:c.1230G>C
|
ENSP00000490471.1:p.Ter410Tyr
|
|
ENST00000637937.1:n.547G>C
|
|
|
ENST00000678991.1:c.*1100G>C
|
ENSP00000503019.1:n.*1100G>C
|
|
ENST00000236671.6:c.1239G>C
|
ENSP00000236671.2:p.Ter413Tyr
|
|
ENST00000427721.2:c.471+300G>C
|
ENSP00000415840.2:n.471+300G>C
|
|
ENST00000429746.1:c.570G>C
|
ENSP00000402586.1:p.Ter190Tyr
|
|
ENST00000433655.5:c.*405G>C
|
ENSP00000404902.1:n.*405G>C
|
|
NM_001909.4:c.1239G>C
|
NP_001900.1:p.Ter413Tyr
|
|
NM_001909.5:c.1239G>C
MANE Select
|
NP_001900.1:p.Ter413Tyr
|
|