ENST00000695651.1:n.2034A>G
|
|
|
ENST00000695652.1:c.3563A>G
|
ENSP00000512083.1:p.Asn1188Ser
|
|
ENST00000695653.1:c.1595A>G
|
ENSP00000512084.1:p.Asn532Ser
|
|
ENST00000695654.1:c.2711A>G
|
ENSP00000512085.1:p.Asn904Ser
|
|
ENST00000695655.1:c.2627A>G
|
ENSP00000512086.1:n.2627A>G
|
|
ENST00000695692.1:n.3050A>G
|
|
|
ENST00000245907.11:c.3686A>G
MANE Select
|
ENSP00000245907.4:p.Asn1229Ser
|
|
ENST00000245907.10:c.3686A>G
|
ENSP00000245907.4:p.Asn1229Ser
|
|
ENST00000596238.1:n.129A>G
|
|
|
ENST00000601008.1:c.241+498A>G
|
ENSP00000471384.1:n.241+498A>G
|
|
NM_000064.3:c.3686A>G
|
NP_000055.2:p.Asn1229Ser
|
|
NM_000064.4:c.3686A>G
MANE Select
|
NP_000055.2:p.Asn1229Ser
|
|