ENST00000650516.2:c.1687G>T
|
ENSP00000498052.2:p.Val563Phe
|
|
ENST00000343257.7:c.1687G>T
MANE Select
|
ENSP00000339867.2:p.Val563Phe
|
|
ENST00000432192.6:c.1511G>T
|
|
|
ENST00000343257.6:c.1687G>T
|
ENSP00000339867.2:p.Val563Phe
|
|
NM_000083.2:c.1687G>T
|
NP_000074.2:p.Val563Phe
|
|
NR_046453.1:n.1627G>T
|
|
|
XM_011515781.1:c.1711G>T
|
XP_011514083.1:p.Val571Phe
|
|
XM_011515782.1:c.433G>T
|
XP_011514084.1:p.Val145Phe
|
|
XM_011515782.2:c.433G>T
|
XP_011514084.1:p.Val145Phe
|
|
XM_017011739.1:c.1261G>T
|
XP_016867228.1:p.Val421Phe
|
|
XM_017011740.1:c.1237G>T
|
XP_016867229.1:p.Val413Phe
|
|
NM_000083.3:c.1687G>T
MANE Select
|
NP_000074.3:p.Val563Phe
|
|
NR_046453.2:n.1642G>T
|
|
|