ENST00000650516.2:c.474T>A
|
ENSP00000498052.2:p.Pro158=
|
|
ENST00000343257.7:c.474T>A
MANE Select
|
ENSP00000339867.2:p.Pro158=
|
|
ENST00000432192.6:c.242T>A
|
|
|
ENST00000650516.1:c.474T>A
|
ENSP00000498052.1:p.Pro158=
|
|
ENST00000343257.6:c.474T>A
|
ENSP00000339867.2:p.Pro158=
|
|
NM_000083.2:c.474T>A
|
NP_000074.2:p.Pro158=
|
|
NR_046453.1:n.561T>A
|
|
|
XM_011515781.1:c.474T>A
|
XP_011514083.1:p.Pro158=
|
|
XM_017011739.1:c.181T>A
|
XP_016867228.1:p.Ser61Thr
|
|
XM_017011740.1:c.181T>A
|
XP_016867229.1:p.Ser61Thr
|
|
NM_000083.3:c.474T>A
MANE Select
|
NP_000074.3:p.Pro158=
|
|
NR_046453.2:n.576T>A
|
|
|