ENST00000673913.2:c.*96A=
|
ENSP00000501161.2:n.*96A=
|
|
ENST00000710286.1:c.2113A=
|
ENSP00000518176.1:p.Asn705=
|
|
ENST00000673903.1:c.1381A=
|
ENSP00000501257.1:p.Asn461=
|
|
ENST00000673913.1:c.606A=
|
ENSP00000501161.1:n.606A=
|
|
ENST00000302118.5:c.1756A=
MANE Select
|
ENSP00000303208.5:p.Asn586=
|
|
ENST00000490692.1:n.2302A=
|
|
|
NM_174936.3:c.1756A= , LRG_275t1:c.1756A=
|
NP_777596.2:p.Asn586=
|
|
NR_110451.1:n.1363A=
|
|
|
XM_011541193.1:c.877A=
|
XP_011539495.1:p.Asn293=
|
|
NM_174936.4:c.1756A=
MANE Select
|
NP_777596.2:p.Asn586=
|
|
NR_110451.2:n.1363A=
|
|
|