ENST00000696170.1:c.*410_*414delinsGTCAC
|
ENSP00000512461.1:n.*410_*414delinsGTCAC
|
|
ENST00000696171.1:c.805_809delinsGTCAC
|
ENSP00000512462.1:p.Val269=
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|
ENST00000378588.5:c.901_905delinsGTCAC
MANE Select
|
ENSP00000367851.4:p.Val301=
|
|
ENST00000378588.4:c.901_905delinsGTCAC
|
ENSP00000367851.4:p.Val301=
|
|
ENST00000465127.1:c.171+377880_171+377884delinsGTCAC
|
ENSP00000417050.1:n.171+377880_171+377884...
|
|
ENST00000492288.1:n.326_330delinsGTCAC
|
|
|
NM_000397.3:c.901_905delinsGTCAC , LRG_53t1:c.901_905delinsGTCAC
|
NP_000388.2:p.Val301=
|
|
XM_011543890.1:c.595_599delinsGTCAC
|
XP_011542192.1:p.Val199=
|
|
NM_000397.4:c.901_905delinsGTCAC
MANE Select
|
NP_000388.2:p.Val301=
|
|