ENST00000673913.2:c.1638G>C
|
ENSP00000501161.2:p.Met546Ile
|
|
ENST00000710286.1:c.1995G>C
|
ENSP00000518176.1:p.Met665Ile
|
|
ENST00000673903.1:c.1263G>C
|
ENSP00000501257.1:p.Met421Ile
|
|
ENST00000673913.1:c.378G>C
|
ENSP00000501161.1:p.Met126Ile
|
|
ENST00000302118.5:c.1638G>C
MANE Select
|
ENSP00000303208.5:p.Met546Ile
|
|
ENST00000490692.1:n.2227+973G>C
|
|
|
NM_174936.3:c.1638G>C , LRG_275t1:c.1638G>C
|
NP_777596.2:p.Met546Ile
|
|
NR_110451.1:n.1245G>C
|
|
|
XM_011541193.1:c.759G>C
|
XP_011539495.1:p.Met253Ile
|
|
NM_174936.4:c.1638G>C
MANE Select
|
NP_777596.2:p.Met546Ile
|
|
NR_110451.2:n.1245G>C
|
|
|