ENST00000261921.8:c.966G>T
(LOXL1)
MANE Select
|
ENSP00000261921.7:p.Gly322=
|
|
ENST00000261921.7:c.966G>T
(LOXL1)
|
ENSP00000261921.7:p.Gly322=
|
|
ENST00000566011.5:c.966G>T
(LOXL1)
|
ENSP00000457827.1:p.Gly322=
|
|
NM_005576.2:c.966G>T
(LOXL1)
|
NP_005567.2:p.Gly322=
|
|
NR_040066.1:n.38C>A
(LOXL1-AS1)
|
|
|
NR_040067.1:n.38C>A
(LOXL1-AS1)
|
|
|
NR_040068.1:n.184+316C>A
(LOXL1-AS1)
|
|
|
NR_040069.1:n.184+316C>A
(LOXL1-AS1)
|
|
|
NR_040070.1:n.184+28C>A
(LOXL1-AS1)
|
|
|
XM_011521555.1:c.966G>T
(LOXL1)
|
XP_011519857.1:p.Gly322=
|
|
XR_931824.1:n.1299G>T
(LOXL1)
|
|
|
NM_005576.3:c.966G>T
(LOXL1)
|
NP_005567.2:p.Gly322=
|
|
XM_011521555.2:c.966G>T
(LOXL1)
|
XP_011519857.1:p.Gly322=
|
|
XR_931824.2:n.1288G>T
(LOXL1)
|
|
|
NM_005576.4:c.966G>T
(LOXL1)
MANE Select
|
NP_005567.2:p.Gly322=
|
|