ENST00000650516.2:c.2653G>A
|
ENSP00000498052.2:p.Ala885Thr
|
|
ENST00000343257.7:c.2653G>A
MANE Select
|
ENSP00000339867.2:p.Ala885Thr
|
|
ENST00000432192.6:c.2477G>A
|
|
|
ENST00000343257.6:c.2653G>A
|
ENSP00000339867.2:p.Ala885Thr
|
|
NM_000083.2:c.2653G>A
|
NP_000074.2:p.Ala885Thr
|
|
NR_046453.1:n.2593G>A
|
|
|
XM_011515781.1:c.2677G>A
|
XP_011514083.1:p.Ala893Thr
|
|
XM_011515782.1:c.1399G>A
|
XP_011514084.1:p.Ala467Thr
|
|
XM_011515782.2:c.1399G>A
|
XP_011514084.1:p.Ala467Thr
|
|
XM_017011739.1:c.2227G>A
|
XP_016867228.1:p.Ala743Thr
|
|
XM_017011740.1:c.2203G>A
|
XP_016867229.1:p.Ala735Thr
|
|
NM_000083.3:c.2653G>A
MANE Select
|
NP_000074.3:p.Ala885Thr
|
|
NR_046453.2:n.2608G>A
|
|
|