ENST00000650516.2:c.1635T>A
|
ENSP00000498052.2:p.Ile545=
|
|
ENST00000343257.7:c.1635T>A
MANE Select
|
ENSP00000339867.2:p.Ile545=
|
|
ENST00000432192.6:c.1459T>A
|
|
|
ENST00000343257.6:c.1635T>A
|
ENSP00000339867.2:p.Ile545=
|
|
NM_000083.2:c.1635T>A
|
NP_000074.2:p.Ile545=
|
|
NR_046453.1:n.1575T>A
|
|
|
XM_011515781.1:c.1659T>A
|
XP_011514083.1:p.Ile553=
|
|
XM_011515782.1:c.381T>A
|
XP_011514084.1:p.Ile127=
|
|
XM_011515782.2:c.381T>A
|
XP_011514084.1:p.Ile127=
|
|
XM_017011739.1:c.1209T>A
|
XP_016867228.1:p.Ile403=
|
|
XM_017011740.1:c.1185T>A
|
XP_016867229.1:p.Ile395=
|
|
NM_000083.3:c.1635T>A
MANE Select
|
NP_000074.3:p.Ile545=
|
|
NR_046453.2:n.1590T>A
|
|
|