ENST00000684241.1:n.1817C>A
|
|
|
ENST00000262186.10:c.984C>A
MANE Select
|
ENSP00000262186.5:p.Arg328=
|
|
ENST00000262186.9:c.984C>A
|
ENSP00000262186.5:p.Arg328=
|
|
ENST00000430723.4:c.636C>A
|
ENSP00000387657.4:p.Arg212=
|
|
ENST00000532957.5:n.1207C>A
|
|
|
NM_000238.3:c.984C>A , LRG_288t1:c.984C>A
|
NP_000229.1:p.Arg328=
|
|
NM_172056.2:c.984C>A , LRG_288t2:c.984C>A
|
NP_742053.1:p.Arg328=
|
|
XM_011516185.1:c.684C>A
|
XP_011514487.1:p.Arg228=
|
|
XM_011516186.1:c.984C>A
|
XP_011514488.1:p.Arg328=
|
|
XM_011516185.2:c.684C>A
|
XP_011514487.1:p.Arg228=
|
|
XM_011516186.3:c.984C>A
|
XP_011514488.1:p.Arg328=
|
|
XM_017012195.1:c.834C>A
|
XP_016867684.1:p.Arg278=
|
|
XM_017012196.1:c.807C>A
|
XP_016867685.1:p.Arg269=
|
|
NM_000238.4:c.984C>A
MANE Select
|
NP_000229.1:p.Arg328=
|
|