ENST00000650516.2:c.1277C>T
|
ENSP00000498052.2:p.Thr426Ile
|
|
ENST00000343257.7:c.1277C>T
MANE Select
|
ENSP00000339867.2:p.Thr426Ile
|
|
ENST00000432192.6:c.1101C>T
|
|
|
ENST00000343257.6:c.1277C>T
|
ENSP00000339867.2:p.Thr426Ile
|
|
NM_000083.2:c.1277C>T
|
NP_000074.2:p.Thr426Ile
|
|
NR_046453.1:n.1341+246C>T
|
|
|
XM_011515781.1:c.1301C>T
|
XP_011514083.1:p.Thr434Ile
|
|
XM_011515782.1:c.23C>T
|
XP_011514084.1:p.Thr8Ile
|
|
XM_011515782.2:c.23C>T
|
XP_011514084.1:p.Thr8Ile
|
|
XM_017011739.1:c.851C>T
|
XP_016867228.1:p.Thr284Ile
|
|
XM_017011740.1:c.827C>T
|
XP_016867229.1:p.Thr276Ile
|
|
NM_000083.3:c.1277C>T
MANE Select
|
NP_000074.3:p.Thr426Ile
|
|
NR_046453.2:n.1356+246C>T
|
|
|