ENST00000578493.2:n.880A>G
|
|
|
ENST00000699291.1:c.672A>G
|
ENSP00000514272.1:n.672A>G
|
|
ENST00000699292.1:n.587A>G
|
|
|
ENST00000225275.4:c.1547A>G
MANE Select
|
ENSP00000225275.3:p.Tyr516Cys
|
|
ENST00000225275.3:c.1547A>G
|
ENSP00000225275.3:p.Tyr516Cys
|
|
ENST00000577220.1:c.5A>G
|
ENSP00000464668.1:p.Tyr2Cys
|
|
NM_000250.1:c.1547A>G , LRG_84t1:c.1547A>G
|
NP_000241.1:p.Tyr516Cys
|
|
XM_011524821.1:c.1733A>G
|
XP_011523123.1:p.Tyr578Cys
|
|
XM_011524822.1:c.1262A>G
|
XP_011523124.1:p.Tyr421Cys
|
|
XM_011524823.1:c.*96A>G
|
XP_011523125.1:n.*96A>G
|
|
NM_000250.2:c.1547A>G
MANE Select
|
NP_000241.1:p.Tyr516Cys
|
|