ENST00000695651.1:n.2002C>T
|
|
|
ENST00000695652.1:c.3531C>T
|
ENSP00000512083.1:p.Asn1177=
|
|
ENST00000695653.1:c.1563C>T
|
ENSP00000512084.1:p.Asn521=
|
|
ENST00000695654.1:c.2679C>T
|
ENSP00000512085.1:p.Asn893=
|
|
ENST00000695655.1:c.2595C>T
|
ENSP00000512086.1:n.2595C>T
|
|
ENST00000695692.1:n.3018C>T
|
|
|
ENST00000245907.11:c.3654C>T
MANE Select
|
ENSP00000245907.4:p.Asn1218=
|
|
ENST00000245907.10:c.3654C>T
|
ENSP00000245907.4:p.Asn1218=
|
|
ENST00000596238.1:n.97C>T
|
|
|
ENST00000601008.1:c.241+466C>T
|
ENSP00000471384.1:n.241+466C>T
|
|
NM_000064.3:c.3654C>T
|
NP_000055.2:p.Asn1218=
|
|
NM_000064.4:c.3654C>T
MANE Select
|
NP_000055.2:p.Asn1218=
|
|