ENST00000395796.8:c.*1293_*1295delinsGCCG
|
ENSP00000379142.4:n.*1293_*1295delinsGCCG
|
|
ENST00000616242.5:c.*415_*417delinsGCCG
|
ENSP00000482149.2:n.*415_*417delinsGCCG
|
|
ENST00000683378.1:n.521_523delinsGCCG
|
|
|
ENST00000336642.9:c.329_331delinsGCCG
|
ENSP00000338009.5:p.Pro110ArgfsTer27
|
|
ENST00000345378.7:c.1298_1300delinsGCCG
|
ENSP00000223366.2:p.Pro433ArgfsTer27
|
|
ENST00000403799.8:c.1295_1297delinsGCCG
MANE Select
|
ENSP00000384247.3:p.Pro432ArgfsTer27
|
|
ENST00000671824.1:c.1358_1360delinsGCCG
|
ENSP00000500264.1:p.Pro453ArgfsTer27
|
|
ENST00000672743.1:n.307_309delinsGCCG
|
|
|
ENST00000673284.1:c.1295_1297delinsGCCG
|
ENSP00000499852.1:p.Pro432ArgfsTer?
|
|
ENST00000336642.8:c.347_349delinsGCCG
|
ENSP00000338009.4:p.Pro116ArgfsTer27
|
|
ENST00000345378.6:c.1298_1300delinsGCCG
|
ENSP00000223366.2:p.Pro433ArgfsTer27
|
|
ENST00000395796.7:c.1292_1294delinsGCCG
|
ENSP00000379142.3:p.Pro431ArgfsTer27
|
|
ENST00000403799.7:c.1295_1297delinsGCCG
|
ENSP00000384247.3:p.Pro432ArgfsTer27
|
|
ENST00000437084.1:c.1244_1246delinsGCCG
|
ENSP00000402840.1:p.Pro415ArgfsTer27
|
|
ENST00000459642.1:n.675_677delinsGCCG
|
|
|
ENST00000616242.4:c.1292_1294delinsGCCG
|
ENSP00000482149.1:p.Pro431ArgfsTer27
|
|
NM_000162.3:c.1295_1297delinsGCCG
|
NP_000153.1:p.Pro432ArgfsTer27
|
|
NM_033507.1:c.1298_1300delinsGCCG
|
NP_277042.1:p.Pro433ArgfsTer27
|
|
NM_033508.1:c.1292_1294delinsGCCG
|
NP_277043.1:p.Pro431ArgfsTer27
|
|
NM_000162.4:c.1295_1297delinsGCCG
|
NP_000153.1:p.Pro432ArgfsTer27
|
|
NM_001354800.1:c.1295_1297delinsGCCG
|
NP_001341729.1:p.Pro432ArgfsTer?
|
|
NM_001354801.1:c.284_286delinsGCCG
|
NP_001341730.1:p.Pro95ArgfsTer27
|
|
NM_001354802.1:c.155_157delinsGCCG
|
NP_001341731.1:p.Pro52ArgfsTer?
|
|
NM_001354803.1:c.329_331delinsGCCG
|
NP_001341732.1:p.Pro110ArgfsTer27
|
|
NM_033507.2:c.1298_1300delinsGCCG
|
NP_277042.1:p.Pro433ArgfsTer27
|
|
NM_033508.2:c.1292_1294delinsGCCG
|
NP_277043.1:p.Pro431ArgfsTer27
|
|
XM_024446707.1:c.155_157delinsGCCG
|
XP_024302475.1:p.Pro52ArgfsTer27
|
|
NM_000162.5:c.1295_1297delinsGCCG
MANE Select
|
NP_000153.1:p.Pro432ArgfsTer27
|
|
NM_033507.3:c.1298_1300delinsGCCG
|
NP_277042.1:p.Pro433ArgfsTer27
|
|
NM_033508.3:c.1292_1294delinsGCCG
|
NP_277043.1:p.Pro431ArgfsTer27
|
|
NM_001354803.2:c.329_331delinsGCCG
|
NP_001341732.1:p.Pro110ArgfsTer27
|
|