ENST00000650516.2:c.*4C>G
|
ENSP00000498052.2:n.*4C>G
|
|
ENST00000343257.7:c.*4C>G
MANE Select
|
ENSP00000339867.2:n.*4C>G
|
|
ENST00000343257.6:c.*4C>G
|
ENSP00000339867.2:n.*4C>G
|
|
NM_000083.2:c.*4C>G
|
NP_000074.2:n.*4C>G
|
|
NR_046453.1:n.2911C>G
|
|
|
XM_011515781.1:c.*4C>G
|
XP_011514083.1:n.*4C>G
|
|
XM_011515782.1:c.*4C>G
|
XP_011514084.1:n.*4C>G
|
|
XM_011515782.2:c.*4C>G
|
XP_011514084.1:n.*4C>G
|
|
XM_017011739.1:c.*4C>G
|
XP_016867228.1:n.*4C>G
|
|
XM_017011740.1:c.*4C>G
|
XP_016867229.1:n.*4C>G
|
|
NM_000083.3:c.*4C>G
MANE Select
|
NP_000074.3:n.*4C>G
|
|
NR_046453.2:n.2926C>G
|
|
|