ENST00000650516.2:c.2907C>T
|
ENSP00000498052.2:p.Ile969=
|
|
ENST00000343257.7:c.2907C>T
MANE Select
|
ENSP00000339867.2:p.Ile969=
|
|
ENST00000343257.6:c.2907C>T
|
ENSP00000339867.2:p.Ile969=
|
|
NM_000083.2:c.2907C>T
|
NP_000074.2:p.Ile969=
|
|
NR_046453.1:n.2847C>T
|
|
|
XM_011515781.1:c.2931C>T
|
XP_011514083.1:p.Ile977=
|
|
XM_011515782.1:c.1653C>T
|
XP_011514084.1:p.Ile551=
|
|
XM_011515782.2:c.1653C>T
|
XP_011514084.1:p.Ile551=
|
|
XM_017011739.1:c.2481C>T
|
XP_016867228.1:p.Ile827=
|
|
XM_017011740.1:c.2457C>T
|
XP_016867229.1:p.Ile819=
|
|
NM_000083.3:c.2907C>T
MANE Select
|
NP_000074.3:p.Ile969=
|
|
NR_046453.2:n.2862C>T
|
|
|