ENST00000650516.2:c.1512G>A
|
ENSP00000498052.2:p.Met504Ile
|
|
ENST00000343257.7:c.1512G>A
MANE Select
|
ENSP00000339867.2:p.Met504Ile
|
|
ENST00000432192.6:c.1336G>A
|
|
|
ENST00000343257.6:c.1512G>A
|
ENSP00000339867.2:p.Met504Ile
|
|
NM_000083.2:c.1512G>A
|
NP_000074.2:p.Met504Ile
|
|
NR_046453.1:n.1452G>A
|
|
|
XM_011515781.1:c.1536G>A
|
XP_011514083.1:p.Met512Ile
|
|
XM_011515782.1:c.258G>A
|
XP_011514084.1:p.Met86Ile
|
|
XM_011515782.2:c.258G>A
|
XP_011514084.1:p.Met86Ile
|
|
XM_017011739.1:c.1086G>A
|
XP_016867228.1:p.Met362Ile
|
|
XM_017011740.1:c.1062G>A
|
XP_016867229.1:p.Met354Ile
|
|
NM_000083.3:c.1512G>A
MANE Select
|
NP_000074.3:p.Met504Ile
|
|
NR_046453.2:n.1467G>A
|
|
|