ENST00000673913.2:c.*108G>C
|
ENSP00000501161.2:n.*108G>C
|
|
ENST00000710286.1:c.2125G>C
|
ENSP00000518176.1:p.Gly709Arg
|
|
ENST00000673903.1:c.1393G>C
|
ENSP00000501257.1:p.Gly465Arg
|
|
ENST00000673913.1:c.618G>C
|
ENSP00000501161.1:n.618G>C
|
|
ENST00000302118.5:c.1768G>C
MANE Select
|
ENSP00000303208.5:p.Gly590Arg
|
|
ENST00000490692.1:n.2314G>C
|
|
|
NM_174936.3:c.1768G>C , LRG_275t1:c.1768G>C
|
NP_777596.2:p.Gly590Arg
|
|
NR_110451.1:n.1375G>C
|
|
|
XM_011541193.1:c.889G>C
|
XP_011539495.1:p.Gly297Arg
|
|
NM_174936.4:c.1768G>C
MANE Select
|
NP_777596.2:p.Gly590Arg
|
|
NR_110451.2:n.1375G>C
|
|
|