ENST00000673913.2:c.*142G>C
|
ENSP00000501161.2:n.*142G>C
|
|
ENST00000710286.1:c.2159G>C
|
ENSP00000518176.1:p.Cys720Ser
|
|
ENST00000673903.1:c.1427G>C
|
ENSP00000501257.1:p.Cys476Ser
|
|
ENST00000673913.1:c.652G>C
|
ENSP00000501161.1:n.652G>C
|
|
ENST00000302118.5:c.1802G>C
MANE Select
|
ENSP00000303208.5:p.Cys601Ser
|
|
ENST00000490692.1:n.2348G>C
|
|
|
NM_174936.3:c.1802G>C , LRG_275t1:c.1802G>C
|
NP_777596.2:p.Cys601Ser
|
|
NR_110451.1:n.1409G>C
|
|
|
XM_011541193.1:c.923G>C
|
XP_011539495.1:p.Cys308Ser
|
|
NM_174936.4:c.1802G>C
MANE Select
|
NP_777596.2:p.Cys601Ser
|
|
NR_110451.2:n.1409G>C
|
|
|