ENST00000650516.2:c.1460T>A
|
ENSP00000498052.2:p.Val487Glu
|
|
ENST00000343257.7:c.1460T>A
MANE Select
|
ENSP00000339867.2:p.Val487Glu
|
|
ENST00000432192.6:c.1284T>A
|
|
|
ENST00000343257.6:c.1460T>A
|
ENSP00000339867.2:p.Val487Glu
|
|
NM_000083.2:c.1460T>A
|
NP_000074.2:p.Val487Glu
|
|
NR_046453.1:n.1400T>A
|
|
|
XM_011515781.1:c.1484T>A
|
XP_011514083.1:p.Val495Glu
|
|
XM_011515782.1:c.206T>A
|
XP_011514084.1:p.Val69Glu
|
|
XM_011515782.2:c.206T>A
|
XP_011514084.1:p.Val69Glu
|
|
XM_017011739.1:c.1034T>A
|
XP_016867228.1:p.Val345Glu
|
|
XM_017011740.1:c.1010T>A
|
XP_016867229.1:p.Val337Glu
|
|
NM_000083.3:c.1460T>A
MANE Select
|
NP_000074.3:p.Val487Glu
|
|
NR_046453.2:n.1415T>A
|
|
|