ENST00000684241.1:n.1610C=
|
|
|
ENST00000262186.10:c.777C=
MANE Select
|
ENSP00000262186.5:p.Asp259=
|
|
ENST00000262186.9:c.777C=
|
ENSP00000262186.5:p.Asp259=
|
|
ENST00000430723.4:c.429C=
|
ENSP00000387657.4:p.Asp143=
|
|
ENST00000532957.5:n.1000C=
|
|
|
NM_000238.3:c.777C= , LRG_288t1:c.777C=
|
NP_000229.1:p.Asp259=
|
|
NM_172056.2:c.777C= , LRG_288t2:c.777C=
|
NP_742053.1:p.Asp259=
|
|
XM_011516185.1:c.477C=
|
XP_011514487.1:p.Asp159=
|
|
XM_011516186.1:c.777C=
|
XP_011514488.1:p.Asp259=
|
|
XM_011516185.2:c.477C=
|
XP_011514487.1:p.Asp159=
|
|
XM_011516186.3:c.777C=
|
XP_011514488.1:p.Asp259=
|
|
XM_017012195.1:c.627C=
|
XP_016867684.1:p.Asp209=
|
|
XM_017012196.1:c.600C=
|
XP_016867685.1:p.Asp200=
|
|
NM_000238.4:c.777C=
MANE Select
|
NP_000229.1:p.Asp259=
|
|