ENST00000695651.1:n.2120G>C
|
|
|
ENST00000695652.1:c.3649G>C
|
ENSP00000512083.1:p.Glu1217Gln
|
|
ENST00000695653.1:c.1681G>C
|
ENSP00000512084.1:p.Glu561Gln
|
|
ENST00000695654.1:c.2797G>C
|
ENSP00000512085.1:p.Glu933Gln
|
|
ENST00000695655.1:c.2713G>C
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ENSP00000512086.1:n.2713G>C
|
|
ENST00000695692.1:n.3136G>C
|
|
|
ENST00000245907.11:c.3772G>C
MANE Select
|
ENSP00000245907.4:p.Glu1258Gln
|
|
ENST00000245907.10:c.3772G>C
|
ENSP00000245907.4:p.Glu1258Gln
|
|
ENST00000596238.1:n.215G>C
|
|
|
ENST00000601008.1:c.241+584G>C
|
ENSP00000471384.1:n.241+584G>C
|
|
NM_000064.3:c.3772G>C
|
NP_000055.2:p.Glu1258Gln
|
|
NM_000064.4:c.3772G>C
MANE Select
|
NP_000055.2:p.Glu1258Gln
|
|