ENST00000695651.1:n.2039G>C
|
|
|
ENST00000695652.1:c.3568G>C
|
ENSP00000512083.1:p.Glu1190Gln
|
|
ENST00000695653.1:c.1600G>C
|
ENSP00000512084.1:p.Glu534Gln
|
|
ENST00000695654.1:c.2716G>C
|
ENSP00000512085.1:p.Glu906Gln
|
|
ENST00000695655.1:c.2632G>C
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ENSP00000512086.1:n.2632G>C
|
|
ENST00000695692.1:n.3055G>C
|
|
|
ENST00000245907.11:c.3691G>C
MANE Select
|
ENSP00000245907.4:p.Glu1231Gln
|
|
ENST00000245907.10:c.3691G>C
|
ENSP00000245907.4:p.Glu1231Gln
|
|
ENST00000596238.1:n.134G>C
|
|
|
ENST00000601008.1:c.241+503G>C
|
ENSP00000471384.1:n.241+503G>C
|
|
NM_000064.3:c.3691G>C
|
NP_000055.2:p.Glu1231Gln
|
|
NM_000064.4:c.3691G>C
MANE Select
|
NP_000055.2:p.Glu1231Gln
|
|