ENST00000236671.7:c.1217T>A
MANE Select
|
ENSP00000236671.2:p.Phe406Tyr
|
|
ENST00000367196.4:c.1112T>A
|
ENSP00000356164.4:p.Phe371Tyr
|
|
ENST00000427721.3:c.634+8T>A
|
|
|
ENST00000429746.2:c.1112T>A
|
ENSP00000402586.2:p.Phe371Tyr
|
|
ENST00000433655.6:c.*383T>A
|
ENSP00000404902.1:n.*383T>A
|
|
ENST00000438213.6:c.1334T>A
|
ENSP00000415036.2:p.Phe445Tyr
|
|
ENST00000636397.1:c.1071+278T>A
|
ENSP00000489910.1:n.1071+278T>A
|
|
ENST00000636571.1:c.1196T>A
|
ENSP00000490770.1:p.Phe399Tyr
|
|
ENST00000636579.1:c.72+278T>A
|
ENSP00000490489.1:n.72+278T>A
|
|
ENST00000636615.1:c.1071+278T>A
|
ENSP00000490014.1:n.1071+278T>A
|
|
ENST00000636843.1:c.1211T>A
|
ENSP00000490897.1:p.Phe404Tyr
|
|
ENST00000637158.1:n.815T>A
|
|
|
ENST00000637381.2:n.3645T>A
|
|
|
ENST00000637387.1:c.1196T>A
|
ENSP00000490598.1:p.Phe399Tyr
|
|
ENST00000637815.2:c.1199T>A
|
ENSP00000490344.1:p.Phe400Tyr
|
|
ENST00000637915.1:c.1208T>A
|
ENSP00000490471.1:p.Phe403Tyr
|
|
ENST00000637937.1:n.525T>A
|
|
|
ENST00000678991.1:c.*1078T>A
|
ENSP00000503019.1:n.*1078T>A
|
|
ENST00000236671.6:c.1217T>A
|
ENSP00000236671.2:p.Phe406Tyr
|
|
ENST00000427721.2:c.471+278T>A
|
ENSP00000415840.2:n.471+278T>A
|
|
ENST00000429746.1:c.548T>A
|
ENSP00000402586.1:p.Phe183Tyr
|
|
ENST00000433655.5:c.*383T>A
|
ENSP00000404902.1:n.*383T>A
|
|
NM_001909.4:c.1217T>A
|
NP_001900.1:p.Phe406Tyr
|
|
NM_001909.5:c.1217T>A
MANE Select
|
NP_001900.1:p.Phe406Tyr
|
|