ENST00000673913.2:c.*184T>A
|
ENSP00000501161.2:n.*184T>A
|
|
ENST00000710286.1:c.2201T>A
|
ENSP00000518176.1:p.Ile734Asn
|
|
ENST00000673903.1:c.1469T>A
|
ENSP00000501257.1:p.Ile490Asn
|
|
ENST00000673913.1:c.694T>A
|
ENSP00000501161.1:n.694T>A
|
|
ENST00000302118.5:c.1844T>A
MANE Select
|
ENSP00000303208.5:p.Ile615Asn
|
|
ENST00000490692.1:n.2390T>A
|
|
|
NM_174936.3:c.1844T>A , LRG_275t1:c.1844T>A
|
NP_777596.2:p.Ile615Asn
|
|
NR_110451.1:n.1451T>A
|
|
|
XM_011541193.1:c.965T>A
|
XP_011539495.1:p.Ile322Asn
|
|
NM_174936.4:c.1844T>A
MANE Select
|
NP_777596.2:p.Ile615Asn
|
|
NR_110451.2:n.1451T>A
|
|
|