ENST00000673913.2:c.1611C>A
|
ENSP00000501161.2:p.His537Gln
|
|
ENST00000710286.1:c.1968C>A
|
ENSP00000518176.1:p.His656Gln
|
|
ENST00000673903.1:c.1236C>A
|
ENSP00000501257.1:p.His412Gln
|
|
ENST00000673913.1:c.351C>A
|
ENSP00000501161.1:p.His117Gln
|
|
ENST00000302118.5:c.1611C>A
MANE Select
|
ENSP00000303208.5:p.His537Gln
|
|
ENST00000490692.1:n.2227+946C>A
|
|
|
NM_174936.3:c.1611C>A , LRG_275t1:c.1611C>A
|
NP_777596.2:p.His537Gln
|
|
NR_110451.1:n.1218C>A
|
|
|
XM_011541193.1:c.732C>A
|
XP_011539495.1:p.His244Gln
|
|
NM_174936.4:c.1611C>A
MANE Select
|
NP_777596.2:p.His537Gln
|
|
NR_110451.2:n.1218C>A
|
|
|