ENST00000650516.2:c.1654C>T
|
ENSP00000498052.2:p.Gln552Ter
|
|
ENST00000343257.7:c.1654C>T
MANE Select
|
ENSP00000339867.2:p.Gln552Ter
|
|
ENST00000432192.6:c.1478C>T
|
|
|
ENST00000343257.6:c.1654C>T
|
ENSP00000339867.2:p.Gln552Ter
|
|
NM_000083.2:c.1654C>T
|
NP_000074.2:p.Gln552Ter
|
|
NR_046453.1:n.1594C>T
|
|
|
XM_011515781.1:c.1678C>T
|
XP_011514083.1:p.Gln560Ter
|
|
XM_011515782.1:c.400C>T
|
XP_011514084.1:p.Gln134Ter
|
|
XM_011515782.2:c.400C>T
|
XP_011514084.1:p.Gln134Ter
|
|
XM_017011739.1:c.1228C>T
|
XP_016867228.1:p.Gln410Ter
|
|
XM_017011740.1:c.1204C>T
|
XP_016867229.1:p.Gln402Ter
|
|
NM_000083.3:c.1654C>T
MANE Select
|
NP_000074.3:p.Gln552Ter
|
|
NR_046453.2:n.1609C>T
|
|
|