ENST00000673913.2:c.1637T>C
|
ENSP00000501161.2:p.Met546Thr
|
|
ENST00000710286.1:c.1994T>C
|
ENSP00000518176.1:p.Met665Thr
|
|
ENST00000673903.1:c.1262T>C
|
ENSP00000501257.1:p.Met421Thr
|
|
ENST00000673913.1:c.377T>C
|
ENSP00000501161.1:p.Met126Thr
|
|
ENST00000302118.5:c.1637T>C
MANE Select
|
ENSP00000303208.5:p.Met546Thr
|
|
ENST00000490692.1:n.2227+972T>C
|
|
|
NM_174936.3:c.1637T>C , LRG_275t1:c.1637T>C
|
NP_777596.2:p.Met546Thr
|
|
NR_110451.1:n.1244T>C
|
|
|
XM_011541193.1:c.758T>C
|
XP_011539495.1:p.Met253Thr
|
|
NM_174936.4:c.1637T>C
MANE Select
|
NP_777596.2:p.Met546Thr
|
|
NR_110451.2:n.1244T>C
|
|
|