ENST00000695651.1:n.2018G=
|
|
|
ENST00000695652.1:c.3547G=
|
ENSP00000512083.1:p.Gly1183=
|
|
ENST00000695653.1:c.1579G=
|
ENSP00000512084.1:p.Gly527=
|
|
ENST00000695654.1:c.2695G=
|
ENSP00000512085.1:p.Gly899=
|
|
ENST00000695655.1:c.2611G=
|
ENSP00000512086.1:n.2611G=
|
|
ENST00000695692.1:n.3034G=
|
|
|
ENST00000245907.11:c.3670G=
MANE Select
|
ENSP00000245907.4:p.Gly1224=
|
|
ENST00000245907.10:c.3670G=
|
ENSP00000245907.4:p.Gly1224=
|
|
ENST00000596238.1:n.113G=
|
|
|
ENST00000601008.1:c.241+482G=
|
ENSP00000471384.1:n.241+482G=
|
|
NM_000064.3:c.3670G=
|
NP_000055.2:p.Gly1224=
|
|
NM_000064.4:c.3670G=
MANE Select
|
NP_000055.2:p.Gly1224=
|
|