ENST00000684241.1:n.3485A>T
|
|
|
ENST00000262186.10:c.2652A>T
MANE Select
|
ENSP00000262186.5:p.Gln884His
|
|
ENST00000330883.9:c.1632A>T
|
ENSP00000328531.4:p.Gln544His
|
|
ENST00000262186.9:c.2652A>T
|
ENSP00000262186.5:p.Gln884His
|
|
ENST00000330883.8:c.1632A>T
|
ENSP00000328531.4:p.Gln544His
|
|
NM_000238.3:c.2652A>T , LRG_288t1:c.2652A>T
|
NP_000229.1:p.Gln884His
|
|
NM_172057.2:c.1632A>T , LRG_288t3:c.1632A>T
|
NP_742054.1:p.Gln544His
|
|
XM_011516185.1:c.2352A>T
|
XP_011514487.1:p.Gln784His
|
|
XM_011516186.1:c.2652A>T
|
XP_011514488.1:p.Gln884His
|
|
XM_011516185.2:c.2352A>T
|
XP_011514487.1:p.Gln784His
|
|
XM_011516186.3:c.2652A>T
|
XP_011514488.1:p.Gln884His
|
|
XM_017012195.1:c.2502A>T
|
XP_016867684.1:p.Gln834His
|
|
XM_017012196.1:c.2475A>T
|
XP_016867685.1:p.Gln825His
|
|
NM_000238.4:c.2652A>T
MANE Select
|
NP_000229.1:p.Gln884His
|
|
NM_172057.3:c.1632A>T
|
NP_742054.1:p.Gln544His
|
|