ENST00000650516.2:c.2802T>A
|
ENSP00000498052.2:p.Pro934=
|
|
ENST00000343257.7:c.2802T>A
MANE Select
|
ENSP00000339867.2:p.Pro934=
|
|
ENST00000343257.6:c.2802T>A
|
ENSP00000339867.2:p.Pro934=
|
|
NM_000083.2:c.2802T>A
|
NP_000074.2:p.Pro934=
|
|
NR_046453.1:n.2742T>A
|
|
|
XM_011515781.1:c.2826T>A
|
XP_011514083.1:p.Pro942=
|
|
XM_011515782.1:c.1548T>A
|
XP_011514084.1:p.Pro516=
|
|
XM_011515782.2:c.1548T>A
|
XP_011514084.1:p.Pro516=
|
|
XM_017011739.1:c.2376T>A
|
XP_016867228.1:p.Pro792=
|
|
XM_017011740.1:c.2352T>A
|
XP_016867229.1:p.Pro784=
|
|
NM_000083.3:c.2802T>A
MANE Select
|
NP_000074.3:p.Pro934=
|
|
NR_046453.2:n.2757T>A
|
|
|