ENST00000650516.2:c.2627C=
|
ENSP00000498052.2:p.Ser876=
|
|
ENST00000343257.7:c.2627C=
MANE Select
|
ENSP00000339867.2:p.Ser876=
|
|
ENST00000432192.6:c.2451C=
|
|
|
ENST00000343257.6:c.2627C=
|
ENSP00000339867.2:p.Ser876=
|
|
NM_000083.2:c.2627C=
|
NP_000074.2:p.Ser876=
|
|
NR_046453.1:n.2567C=
|
|
|
XM_011515781.1:c.2651C=
|
XP_011514083.1:p.Ser884=
|
|
XM_011515782.1:c.1373C=
|
XP_011514084.1:p.Ser458=
|
|
XM_011515782.2:c.1373C=
|
XP_011514084.1:p.Ser458=
|
|
XM_017011739.1:c.2201C=
|
XP_016867228.1:p.Ser734=
|
|
XM_017011740.1:c.2177C=
|
XP_016867229.1:p.Ser726=
|
|
NM_000083.3:c.2627C=
MANE Select
|
NP_000074.3:p.Ser876=
|
|
NR_046453.2:n.2582C=
|
|
|