ENST00000650516.2:c.2711C>T
|
ENSP00000498052.2:p.Ala904Val
|
|
ENST00000343257.7:c.2711C>T
MANE Select
|
ENSP00000339867.2:p.Ala904Val
|
|
ENST00000432192.6:c.2535C>T
|
|
|
ENST00000343257.6:c.2711C>T
|
ENSP00000339867.2:p.Ala904Val
|
|
NM_000083.2:c.2711C>T
|
NP_000074.2:p.Ala904Val
|
|
NR_046453.1:n.2651C>T
|
|
|
XM_011515781.1:c.2735C>T
|
XP_011514083.1:p.Ala912Val
|
|
XM_011515782.1:c.1457C>T
|
XP_011514084.1:p.Ala486Val
|
|
XM_011515782.2:c.1457C>T
|
XP_011514084.1:p.Ala486Val
|
|
XM_017011739.1:c.2285C>T
|
XP_016867228.1:p.Ala762Val
|
|
XM_017011740.1:c.2261C>T
|
XP_016867229.1:p.Ala754Val
|
|
NM_000083.3:c.2711C>T
MANE Select
|
NP_000074.3:p.Ala904Val
|
|
NR_046453.2:n.2666C>T
|
|
|