ENST00000650516.2:c.2960T>G
|
ENSP00000498052.2:p.Ile987Ser
|
|
ENST00000343257.7:c.2960T>G
MANE Select
|
ENSP00000339867.2:p.Ile987Ser
|
|
ENST00000343257.6:c.2960T>G
|
ENSP00000339867.2:p.Ile987Ser
|
|
NM_000083.2:c.2960T>G
|
NP_000074.2:p.Ile987Ser
|
|
NR_046453.1:n.2900T>G
|
|
|
XM_011515781.1:c.2984T>G
|
XP_011514083.1:p.Ile995Ser
|
|
XM_011515782.1:c.1706T>G
|
XP_011514084.1:p.Ile569Ser
|
|
XM_011515782.2:c.1706T>G
|
XP_011514084.1:p.Ile569Ser
|
|
XM_017011739.1:c.2534T>G
|
XP_016867228.1:p.Ile845Ser
|
|
XM_017011740.1:c.2510T>G
|
XP_016867229.1:p.Ile837Ser
|
|
NM_000083.3:c.2960T>G
MANE Select
|
NP_000074.3:p.Ile987Ser
|
|
NR_046453.2:n.2915T>G
|
|
|