ENST00000650516.2:c.2959A>T
|
ENSP00000498052.2:p.Ile987Phe
|
|
ENST00000343257.7:c.2959A>T
MANE Select
|
ENSP00000339867.2:p.Ile987Phe
|
|
ENST00000343257.6:c.2959A>T
|
ENSP00000339867.2:p.Ile987Phe
|
|
NM_000083.2:c.2959A>T
|
NP_000074.2:p.Ile987Phe
|
|
NR_046453.1:n.2899A>T
|
|
|
XM_011515781.1:c.2983A>T
|
XP_011514083.1:p.Ile995Phe
|
|
XM_011515782.1:c.1705A>T
|
XP_011514084.1:p.Ile569Phe
|
|
XM_011515782.2:c.1705A>T
|
XP_011514084.1:p.Ile569Phe
|
|
XM_017011739.1:c.2533A>T
|
XP_016867228.1:p.Ile845Phe
|
|
XM_017011740.1:c.2509A>T
|
XP_016867229.1:p.Ile837Phe
|
|
NM_000083.3:c.2959A>T
MANE Select
|
NP_000074.3:p.Ile987Phe
|
|
NR_046453.2:n.2914A>T
|
|
|