ENST00000684241.1:n.3593G>T
|
|
|
ENST00000262186.10:c.2760G>T
MANE Select
|
ENSP00000262186.5:p.Arg920=
|
|
ENST00000330883.9:c.1740G>T
|
ENSP00000328531.4:p.Arg580=
|
|
ENST00000262186.9:c.2760G>T
|
ENSP00000262186.5:p.Arg920=
|
|
ENST00000330883.8:c.1740G>T
|
ENSP00000328531.4:p.Arg580=
|
|
NM_000238.3:c.2760G>T , LRG_288t1:c.2760G>T
|
NP_000229.1:p.Arg920=
|
|
NM_172057.2:c.1740G>T , LRG_288t3:c.1740G>T
|
NP_742054.1:p.Arg580=
|
|
XM_011516185.1:c.2460G>T
|
XP_011514487.1:p.Arg820=
|
|
XM_011516186.1:c.2693-120G>T
|
XP_011514488.1:n.2693-120G>T
|
|
XM_011516185.2:c.2460G>T
|
XP_011514487.1:p.Arg820=
|
|
XM_011516186.3:c.2693-120G>T
|
XP_011514488.1:n.2693-120G>T
|
|
XM_017012195.1:c.2610G>T
|
XP_016867684.1:p.Arg870=
|
|
XM_017012196.1:c.2583G>T
|
XP_016867685.1:p.Arg861=
|
|
NM_000238.4:c.2760G>T
MANE Select
|
NP_000229.1:p.Arg920=
|
|
NM_172057.3:c.1740G>T
|
NP_742054.1:p.Arg580=
|
|