ENST00000371974.8:c.751+11_751+12delinsGA
MANE Select
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ENSP00000361042.3:n.751+11_751+12delinsGA
|
|
ENST00000371974.7:c.751+11_751+12delinsGA
|
ENSP00000361042.3:n.751+11_751+12delinsGA
|
|
ENST00000437995.1:n.661+11_661+12delinsGA
|
|
|
ENST00000495952.5:n.741+11_741+12delinsGA
|
|
|
ENST00000615505.4:c.424+11_424+12delinsGA
|
ENSP00000482067.1:n.424+11_424+12delinsGA
|
|
NM_001280787.1:c.424+11_424+12delinsGA
|
NP_001267716.1:n.424+11_424+12delinsGA
|
|
NM_003172.3:c.751+11_751+12delinsGA
|
NP_003163.1:n.751+11_751+12delinsGA
|
|
XM_011518942.1:c.424+11_424+12delinsGA
|
XP_011517244.1:n.424+11_424+12delinsGA
|
|
NM_003172.4:c.751+11_751+12delinsGA
MANE Select
|
NP_003163.1:n.751+11_751+12delinsGA
|
|