ENST00000695651.1:n.884G>C
|
|
|
ENST00000695652.1:c.2413G>C
|
ENSP00000512083.1:p.Glu805Gln
|
|
ENST00000695653.1:c.445G>C
|
ENSP00000512084.1:p.Glu149Gln
|
|
ENST00000695654.1:c.1660G>C
|
ENSP00000512085.1:p.Glu554Gln
|
|
ENST00000695655.1:c.1477G>C
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ENSP00000512086.1:n.1477G>C
|
|
ENST00000695692.1:n.1900G>C
|
|
|
ENST00000245907.11:c.2536G>C
MANE Select
|
ENSP00000245907.4:p.Glu846Gln
|
|
ENST00000245907.10:c.2536G>C
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ENSP00000245907.4:p.Glu846Gln
|
|
ENST00000594005.1:n.17G>C
|
|
|
ENST00000602053.1:n.584G>C
|
|
|
NM_000064.3:c.2536G>C
|
NP_000055.2:p.Glu846Gln
|
|
NM_000064.4:c.2536G>C
MANE Select
|
NP_000055.2:p.Glu846Gln
|
|