ENST00000673913.2:c.1599C>G
|
ENSP00000501161.2:p.Asn533Lys
|
|
ENST00000710286.1:c.1956C>G
|
ENSP00000518176.1:p.Asn652Lys
|
|
ENST00000673903.1:c.1224C>G
|
ENSP00000501257.1:p.Asn408Lys
|
|
ENST00000673913.1:c.339C>G
|
ENSP00000501161.1:p.Asn113Lys
|
|
ENST00000302118.5:c.1599C>G
MANE Select
|
ENSP00000303208.5:p.Asn533Lys
|
|
ENST00000490692.1:n.2227+934C>G
|
|
|
NM_174936.3:c.1599C>G , LRG_275t1:c.1599C>G
|
NP_777596.2:p.Asn533Lys
|
|
NR_110451.1:n.1206C>G
|
|
|
XM_011541193.1:c.720C>G
|
XP_011539495.1:p.Asn240Lys
|
|
NM_174936.4:c.1599C>G
MANE Select
|
NP_777596.2:p.Asn533Lys
|
|
NR_110451.2:n.1206C>G
|
|
|