ENST00000261921.8:c.332T>G
(LOXL1)
MANE Select
|
ENSP00000261921.7:p.Val111Gly
|
|
ENST00000261921.7:c.332T>G
(LOXL1)
|
ENSP00000261921.7:p.Val111Gly
|
|
ENST00000566011.5:c.332T>G
(LOXL1)
|
ENSP00000457827.1:p.Val111Gly
|
|
NM_005576.2:c.332T>G
(LOXL1)
|
NP_005567.2:p.Val111Gly
|
|
NR_040066.1:n.133+539A>C
(LOXL1-AS1)
|
|
|
NR_040067.1:n.133+539A>C
(LOXL1-AS1)
|
|
|
NR_040068.1:n.184+950A>C
(LOXL1-AS1)
|
|
|
NR_040069.1:n.184+950A>C
(LOXL1-AS1)
|
|
|
NR_040070.1:n.184+662A>C
(LOXL1-AS1)
|
|
|
XM_011521555.1:c.332T>G
(LOXL1)
|
XP_011519857.1:p.Val111Gly
|
|
XR_931824.1:n.665T>G
(LOXL1)
|
|
|
NM_005576.3:c.332T>G
(LOXL1)
|
NP_005567.2:p.Val111Gly
|
|
XM_011521555.2:c.332T>G
(LOXL1)
|
XP_011519857.1:p.Val111Gly
|
|
XR_931824.2:n.654T>G
(LOXL1)
|
|
|
NM_005576.4:c.332T>G
(LOXL1)
MANE Select
|
NP_005567.2:p.Val111Gly
|
|