|
ENST00000383096.8:c.2524-5359_2524-5358delinsAG
MANE Select
|
ENSP00000372576.3:n.2524-5359_2524-5358delinsAG
|
|
|
ENST00000300227.12:c.2410-5359_2410-5358delinsAG
|
ENSP00000300227.8:n.2410-5359_2410-5358delinsAG
|
|
|
ENST00000383096.7:c.2524-5359_2524-5358delinsAG
|
ENSP00000372576.3:n.2524-5359_2524-5358delinsAG
|
|
|
ENST00000403303.5:c.2524-5359_2524-5358delinsAG
|
ENSP00000385591.1:n.2524-5359_2524-5358delinsAG
|
|
|
ENST00000406524.6:c.2596-5359_2596-5358delinsAG
|
ENSP00000385867.2:n.2596-5359_2596-5358delinsAG
|
|
|
ENST00000579916.5:c.484-5359_484-5358delinsAG
|
ENSP00000462153.1:n.484-5359_484-5358delinsAG
|
|
|
ENST00000581524.5:c.1015-5359_1015-5358delinsAG
|
ENSP00000462651.1:n.1015-5359_1015-5358delinsAG
|
|
|
ENST00000581852.5:c.139-5359_139-5358delinsAG
|
ENSP00000464295.1:n.139-5359_139-5358delinsAG
|
|
|
ENST00000583930.5:c.2596-5359_2596-5358delinsAG
|
ENSP00000463254.1:n.2596-5359_2596-5358delinsAG
|
|
|
NM_001105528.1:c.2524-5359_2524-5358delinsAG
|
NP_001098998.1:n.2524-5359_2524-5358delinsAG
|
|
|
NM_001308126.1:c.2596-5359_2596-5358delinsAG
|
NP_001295055.1:n.2596-5359_2596-5358delinsAG
|
|
|
NM_198995.2:c.2410-5359_2410-5358delinsAG
|
NP_945346.2:n.2410-5359_2410-5358delinsAG
|
|
|
XM_011525948.1:c.2524-5359_2524-5358delinsAG
|
XP_011524250.1:n.2524-5359_2524-5358delinsAG
|
|
|
XM_011525951.1:c.2374-5359_2374-5358delinsAG
|
XP_011524253.1:n.2374-5359_2374-5358delinsAG
|
|
|
XR_935363.1:n.179+5172_179+5173delinsCT
|
|
|
|
XM_017025721.1:c.2596-5359_2596-5358delinsAG
|
XP_016881210.1:n.2596-5359_2596-5358delinsAG
|
|
|
XM_017025722.1:c.2596-5359_2596-5358delinsAG
|
XP_016881211.1:n.2596-5359_2596-5358delinsAG
|
|
|
XM_017025723.1:c.2596-5359_2596-5358delinsAG
|
XP_016881212.1:n.2596-5359_2596-5358delinsAG
|
|
|
XM_017025724.1:c.2110-5359_2110-5358delinsAG
|
XP_016881213.1:n.2110-5359_2110-5358delinsAG
|
|
|
XM_017025725.1:c.2110-5359_2110-5358delinsAG
|
XP_016881214.1:n.2110-5359_2110-5358delinsAG
|
|
|
XR_001753402.1:n.179+5172_179+5173delinsCT
|
|
|
|
XR_935363.2:n.179+5172_179+5173delinsCT
|
|
|
|
XR_935365.2:n.179+5172_179+5173delinsCT
|
|
|
|
NM_001105528.3:c.2524-5359_2524-5358delinsAG
|
NP_001098998.1:n.2524-5359_2524-5358delinsAG
|
|
|
NM_001308126.3:c.2596-5359_2596-5358delinsAG
|
NP_001295055.1:n.2596-5359_2596-5358delinsAG
|
|
|
NM_001371120.1:c.2596-5359_2596-5358delinsAG
|
NP_001358049.1:n.2596-5359_2596-5358delinsAG
|
|
|
NM_001371121.1:c.2596-5359_2596-5358delinsAG
|
NP_001358050.1:n.2596-5359_2596-5358delinsAG
|
|
|
NM_198995.3:c.2410-5359_2410-5358delinsAG
|
NP_945346.2:n.2410-5359_2410-5358delinsAG
|
|
|
NM_001105528.4:c.2524-5359_2524-5358delinsAG
MANE Select
|
NP_001098998.1:n.2524-5359_2524-5358delinsAG
|
|
