NM_002332.3:c.713C>T
(LRP1)
MANE Select
|
NP_002323.2:p.Ala238Val
|
ENST00000243077.8:c.713C>T
(LRP1)
MANE Select
|
ENSP00000243077.3:p.Ala238Val
|
NM_002332.2:c.713C>T
(LRP1)
|
NP_002323.2:p.Ala238Val
|
NR_131938.1:n.182-279G>A
(LRP1-AS)
|
|
ENST00000243077.7:c.713C>T
(LRP1)
|
ENSP00000243077.3:p.Ala238Val
|
ENST00000338962.8:c.713C>T
(LRP1)
|
ENSP00000341264.4:p.Ala238Val
|
ENST00000553277.5:c.713C>T
(LRP1)
|
ENSP00000451449.1:p.Ala238Val
|
ENST00000554174.1:c.713C>T
(LRP1)
|
ENSP00000451737.1:p.Ala238Val
|
XM_017019303.1:c.713C>T
(LRP1)
|
XP_016874792.1:p.Ala238Val
|