ENST00000298171.7:c.1629T>A
MANE Select
|
ENSP00000298171.2:p.Val543=
|
|
ENST00000636454.1:n.1547T>A
|
|
|
ENST00000637447.1:c.532T>A
|
|
|
ENST00000298171.6:c.1629T>A
|
ENSP00000298171.2:p.Val543=
|
|
ENST00000541158.6:c.1629T>A
|
ENSP00000441235.2:p.Val543=
|
|
NM_000369.2:c.1629T>A , LRG_523t1:c.1629T>A
|
NP_000360.2:p.Val543=
|
|
XM_005268037.3:c.1629T>A
|
XP_005268094.1:p.Val543=
|
|
XM_011537119.1:c.1350T>A
|
XP_011535421.1:p.Val450=
|
|
XR_245790.3:n.2086+21506A>T
|
|
|
XR_429385.2:n.853+21506A>T
|
|
|
XR_429386.2:n.854+21506A>T
|
|
|
XR_944075.1:n.865+21506A>T
|
|
|
XR_944076.1:n.861+21506A>T
|
|
|
XR_944077.1:n.865+21506A>T
|
|
|
XR_944078.1:n.865+21506A>T
|
|
|
XR_944079.1:n.855+21506A>T
|
|
|
XM_005268037.4:c.1629T>A
|
XP_005268094.1:p.Val543=
|
|
XM_011537119.2:c.1350T>A
|
XP_011535421.1:p.Val450=
|
|
XR_001751021.1:n.2753+21506A>T
|
|
|
XR_001751022.1:n.2753+21506A>T
|
|
|
XR_001751023.1:n.2753+21506A>T
|
|
|
XR_944075.3:n.929+21506A>T
|
|
|
NM_000369.4:c.1629T>A
|
NP_000360.2:p.Val543=
|
|
NM_000369.5:c.1629T>A
MANE Select
|
NP_000360.2:p.Val543=
|
|