ENST00000673913.2:c.1555G>C
|
ENSP00000501161.2:p.Gly519Arg
|
|
ENST00000710286.1:c.1912G>C
|
ENSP00000518176.1:p.Gly638Arg
|
|
ENST00000673903.1:c.1180G>C
|
ENSP00000501257.1:p.Gly394Arg
|
|
ENST00000673913.1:c.295G>C
|
ENSP00000501161.1:p.Gly99Arg
|
|
ENST00000302118.5:c.1555G>C
MANE Select
|
ENSP00000303208.5:p.Gly519Arg
|
|
ENST00000490692.1:n.2227+890G>C
|
|
|
NM_174936.3:c.1555G>C , LRG_275t1:c.1555G>C
|
NP_777596.2:p.Gly519Arg
|
|
NR_110451.1:n.1162G>C
|
|
|
XM_011541193.1:c.676G>C
|
XP_011539495.1:p.Gly226Arg
|
|
NM_174936.4:c.1555G>C
MANE Select
|
NP_777596.2:p.Gly519Arg
|
|
NR_110451.2:n.1162G>C
|
|
|