ENST00000673913.2:c.1643C>A
|
ENSP00000501161.2:p.Thr548Asn
|
|
ENST00000710286.1:c.2000C>A
|
ENSP00000518176.1:p.Thr667Asn
|
|
ENST00000673903.1:c.1268C>A
|
ENSP00000501257.1:p.Thr423Asn
|
|
ENST00000673913.1:c.383C>A
|
ENSP00000501161.1:p.Thr128Asn
|
|
ENST00000302118.5:c.1643C>A
MANE Select
|
ENSP00000303208.5:p.Thr548Asn
|
|
ENST00000490692.1:n.2227+978C>A
|
|
|
NM_174936.3:c.1643C>A , LRG_275t1:c.1643C>A
|
NP_777596.2:p.Thr548Asn
|
|
NR_110451.1:n.1250C>A
|
|
|
XM_011541193.1:c.764C>A
|
XP_011539495.1:p.Thr255Asn
|
|
NM_174936.4:c.1643C>A
MANE Select
|
NP_777596.2:p.Thr548Asn
|
|
NR_110451.2:n.1250C>A
|
|
|