ENST00000673913.2:c.*101G>T
|
ENSP00000501161.2:n.*101G>T
|
|
ENST00000710286.1:c.2118G>T
|
ENSP00000518176.1:p.Gln706His
|
|
ENST00000673903.1:c.1386G>T
|
ENSP00000501257.1:p.Gln462His
|
|
ENST00000673913.1:c.611G>T
|
ENSP00000501161.1:n.611G>T
|
|
ENST00000302118.5:c.1761G>T
MANE Select
|
ENSP00000303208.5:p.Gln587His
|
|
ENST00000490692.1:n.2307G>T
|
|
|
NM_174936.3:c.1761G>T , LRG_275t1:c.1761G>T
|
NP_777596.2:p.Gln587His
|
|
NR_110451.1:n.1368G>T
|
|
|
XM_011541193.1:c.882G>T
|
XP_011539495.1:p.Gln294His
|
|
NM_174936.4:c.1761G>T
MANE Select
|
NP_777596.2:p.Gln587His
|
|
NR_110451.2:n.1368G>T
|
|
|