ENST00000673913.2:c.1611C=
|
ENSP00000501161.2:p.His537=
|
|
ENST00000710286.1:c.1968C=
|
ENSP00000518176.1:p.His656=
|
|
ENST00000673903.1:c.1236C=
|
ENSP00000501257.1:p.His412=
|
|
ENST00000673913.1:c.351C=
|
ENSP00000501161.1:p.His117=
|
|
ENST00000302118.5:c.1611C=
MANE Select
|
ENSP00000303208.5:p.His537=
|
|
ENST00000490692.1:n.2227+946C=
|
|
|
NM_174936.3:c.1611C= , LRG_275t1:c.1611C=
|
NP_777596.2:p.His537=
|
|
NR_110451.1:n.1218C=
|
|
|
XM_011541193.1:c.732C=
|
XP_011539495.1:p.His244=
|
|
NM_174936.4:c.1611C=
MANE Select
|
NP_777596.2:p.His537=
|
|
NR_110451.2:n.1218C=
|
|
|