ENST00000290866.10:c.2641+231G>C
MANE Select
|
ENSP00000290866.4:n.2641+231G>C
|
|
ENST00000290863.10:c.919+231G>C
|
ENSP00000290863.6:n.919+231G>C
|
|
ENST00000290866.9:c.2641+231G>C
|
ENSP00000290866.4:n.2641+231G>C
|
|
ENST00000413513.7:c.919+231G>C
|
ENSP00000392247.3:n.919+231G>C
|
|
ENST00000428043.5:c.2641+231G>C
|
ENSP00000397593.2:n.2641+231G>C
|
|
ENST00000577647.2:c.919+231G>C
|
ENSP00000464149.1:n.919+231G>C
|
|
ENST00000578839.5:c.*519+572G>C
|
ENSP00000462110.2:n.*519+572G>C
|
|
ENST00000579314.5:c.*370+231G>C
|
ENSP00000462599.1:n.*370+231G>C
|
|
ENST00000582761.1:c.409+231G>C
|
ENSP00000462909.1:n.409+231G>C
|
|
ENST00000584865.5:n.587+231G>C
|
|
|
NM_000789.3:c.2641+231G>C
|
NP_000780.1:n.2641+231G>C
|
|
NM_001178057.1:c.919+231G>C
|
NP_001171528.1:n.919+231G>C
|
|
NM_152830.2:c.919+231G>C
|
NP_690043.1:n.919+231G>C
|
|
XM_005257110.1:c.2092+231G>C
|
XP_005257167.1:n.2092+231G>C
|
|
XM_006721737.2:c.979+231G>C
|
XP_006721800.2:n.979+231G>C
|
|
XM_006721737.3:c.979+231G>C
|
XP_006721800.2:n.979+231G>C
|
|
NM_000789.4:c.2641+231G>C
MANE Select
|
NP_000780.1:n.2641+231G>C
|
|
NM_001178057.2:c.919+231G>C
|
NP_001171528.1:n.919+231G>C
|
|
NM_152830.3:c.919+231G>C
|
NP_690043.1:n.919+231G>C
|
|
NM_001382700.1:c.2074+231G>C
|
NP_001369629.1:n.2074+231G>C
|
|
NM_001382701.1:c.1789+231G>C
|
NP_001369630.1:n.1789+231G>C
|
|
NM_001382702.1:c.379+572G>C
|
NP_001369631.1:n.379+572G>C
|
|
NR_168483.1:n.1019+231G>C
|
|
|