ENST00000292303.5:c.992C>T
(CCR5)
MANE Select
|
ENSP00000292303.4:p.Ala331Val
|
|
ENST00000292303.4:c.992C>T
(CCR5)
|
ENSP00000292303.4:p.Ala331Val
|
|
ENST00000445772.1:c.992C>T
(CCR5)
|
ENSP00000404881.1:p.Ala331Val
|
|
NM_000579.3:c.992C>T
(CCR5)
|
NP_000570.1:p.Ala331Val
|
|
NM_001100168.1:c.992C>T
(CCR5)
|
NP_001093638.1:p.Ala331Val
|
|
NR_125406.1:n.392-2477G>A
(CCR5AS)
|
|
|
NM_000579.4:c.992C>T
(CCR5)
|
NP_000570.1:p.Ala331Val
|
|
NM_001100168.2:c.992C>T
(CCR5)
|
NP_001093638.1:p.Ala331Val
|
|
NM_001394783.1:c.992C>T
(CCR5)
MANE Select
|
NP_001381712.1:p.Ala331Val
|
|