|
ENST00000290866.10:c.3691+3_3691+4insGCC
MANE Select
|
ENSP00000290866.4:n.3691+3_3691+4insGCC
|
|
|
ENST00000290863.10:c.1969+3_1969+4insGCC
|
ENSP00000290863.6:n.1969+3_1969+4insGCC
|
|
|
ENST00000290866.9:c.3691+3_3691+4insGCC
|
ENSP00000290866.4:n.3691+3_3691+4insGCC
|
|
|
ENST00000413513.7:c.1846+3_1846+4insGCC
|
ENSP00000392247.3:n.1846+3_1846+4insGCC
|
|
|
ENST00000428043.5:c.3694_3695insGCC
|
ENSP00000397593.2:p.Thr1232delinsSerPro
|
|
|
ENST00000577418.5:n.701+3_701+4insGCC
|
|
|
|
ENST00000577647.2:c.1969+3_1969+4insGCC
|
ENSP00000464149.1:n.1969+3_1969+4insGCC
|
|
|
ENST00000578839.5:c.*1446+3_*1446+4insGCC
|
ENSP00000462110.2:n.*1446+3_*1446+4insGCC...
|
|
|
ENST00000579314.5:c.*1420+3_*1420+4insGCC
|
ENSP00000462599.1:n.*1420+3_*1420+4insGCC...
|
|
|
ENST00000579409.1:c.381_382insGCC
|
|
|
|
NM_000789.3:c.3691+3_3691+4insGCC
|
NP_000780.1:n.3691+3_3691+4insGCC
|
|
|
NM_001178057.1:c.1846+3_1846+4insGCC
|
NP_001171528.1:n.1846+3_1846+4insGCC
|
|
|
NM_152830.2:c.1969+3_1969+4insGCC
|
NP_690043.1:n.1969+3_1969+4insGCC
|
|
|
XM_005257110.1:c.3142+3_3142+4insGCC
|
XP_005257167.1:n.3142+3_3142+4insGCC
|
|
|
XM_006721737.2:c.2029+3_2029+4insGCC
|
XP_006721800.2:n.2029+3_2029+4insGCC
|
|
|
XM_006721737.3:c.2029+3_2029+4insGCC
|
XP_006721800.2:n.2029+3_2029+4insGCC
|
|
|
NM_000789.4:c.3691+3_3691+4insGCC
MANE Select
|
NP_000780.1:n.3691+3_3691+4insGCC
|
|
|
NM_001178057.2:c.1846+3_1846+4insGCC
|
NP_001171528.1:n.1846+3_1846+4insGCC
|
|
|
NM_152830.3:c.1969+3_1969+4insGCC
|
NP_690043.1:n.1969+3_1969+4insGCC
|
|
|
NM_001382700.1:c.3124+3_3124+4insGCC
|
NP_001369629.1:n.3124+3_3124+4insGCC
|
|
|
NM_001382701.1:c.2839+3_2839+4insGCC
|
NP_001369630.1:n.2839+3_2839+4insGCC
|
|
|
NM_001382702.1:c.1306+3_1306+4insGCC
|
NP_001369631.1:n.1306+3_1306+4insGCC
|
|
|
NR_168483.1:n.2069+3_2069+4insGCC
|
|
|
