ENST00000650516.2:c.1272C>T
|
ENSP00000498052.2:p.Ile424=
|
|
ENST00000343257.7:c.1272C>T
MANE Select
|
ENSP00000339867.2:p.Ile424=
|
|
ENST00000432192.6:c.1096C>T
|
|
|
ENST00000343257.6:c.1272C>T
|
ENSP00000339867.2:p.Ile424=
|
|
NM_000083.2:c.1272C>T
|
NP_000074.2:p.Ile424=
|
|
NR_046453.1:n.1341+241C>T
|
|
|
XM_011515781.1:c.1296C>T
|
XP_011514083.1:p.Ile432=
|
|
XM_011515782.1:c.18C>T
|
XP_011514084.1:p.Ile6=
|
|
XM_011515782.2:c.18C>T
|
XP_011514084.1:p.Ile6=
|
|
XM_017011739.1:c.846C>T
|
XP_016867228.1:p.Ile282=
|
|
XM_017011740.1:c.822C>T
|
XP_016867229.1:p.Ile274=
|
|
NM_000083.3:c.1272C>T
MANE Select
|
NP_000074.3:p.Ile424=
|
|
NR_046453.2:n.1356+241C>T
|
|
|