ENST00000596399.2:c.57G>A
(LIM2)
MANE Select
|
ENSP00000472090.2:p.Leu19=
|
|
ENST00000221973.7:c.57G>A
(LIM2)
|
ENSP00000221973.2:p.Leu19=
|
|
ENST00000596399.1:c.57G>A
(LIM2)
|
ENSP00000472090.1:p.Leu19=
|
|
NM_001161748.1:c.57G>A
(LIM2)
|
NP_001155220.1:p.Leu19=
|
|
NM_030657.3:c.57G>A
(LIM2)
|
NP_085915.2:p.Leu19=
|
|
XR_002958395.1:n.465C>T
(LIM2-AS1)
|
|
|
XR_002958396.1:n.465C>T
(LIM2-AS1)
|
|
|
XR_002958397.1:n.465C>T
(LIM2-AS1)
|
|
|
XR_002958398.1:n.465C>T
(LIM2-AS1)
|
|
|
NM_001161748.2:c.57G>A
(LIM2)
MANE Select
|
NP_001155220.1:p.Leu19=
|
|
NM_030657.4:c.57G>A
(LIM2)
|
NP_085915.2:p.Leu19=
|
|