ENST00000650516.2:c.853+591T>G
|
ENSP00000498052.2:n.853+591T>G
|
|
ENST00000343257.7:c.849T>G
MANE Select
|
ENSP00000339867.2:p.Leu283=
|
|
ENST00000432192.6:c.673T>G
|
|
|
ENST00000455478.6:c.437T>G
|
ENSP00000400027.2:n.437T>G
|
|
ENST00000650516.1:c.853+591T>G
|
ENSP00000498052.1:n.853+591T>G
|
|
ENST00000343257.6:c.849T>G
|
ENSP00000339867.2:p.Leu283=
|
|
ENST00000432192.5:c.363T>G
|
|
|
ENST00000455478.5:c.441T>G
|
|
|
ENST00000495612.1:n.154+2640T>G
|
|
|
NM_000083.2:c.849T>G
|
NP_000074.2:p.Leu283=
|
|
NR_046453.1:n.939T>G
|
|
|
XM_011515781.1:c.853+591T>G
|
XP_011514083.1:n.853+591T>G
|
|
XM_017011739.1:c.403+2640T>G
|
XP_016867228.1:n.403+2640T>G
|
|
XM_017011740.1:c.403+2640T>G
|
XP_016867229.1:n.403+2640T>G
|
|
NM_000083.3:c.849T>G
MANE Select
|
NP_000074.3:p.Leu283=
|
|
NR_046453.2:n.954T>G
|
|
|