ENST00000352511.5:c.110A>T
MANE Select
|
ENSP00000340361.3:p.Glu37Val
|
|
ENST00000352511.4:c.110A>T
|
ENSP00000340361.3:p.Glu37Val
|
|
ENST00000461232.1:n.3899A>T
|
|
|
ENST00000465020.5:n.114A>T
|
|
|
NM_001106.3:c.110A>T
|
NP_001097.2:p.Glu37Val
|
|
XM_005265583.2:c.173A>T
|
XP_005265640.1:p.Glu58Val
|
|
XM_005265583.3:c.173A>T
|
XP_005265640.1:p.Glu58Val
|
|
XM_017007514.1:c.152A>T
|
XP_016863003.1:p.Glu51Val
|
|
XM_017007515.2:c.128A>T
|
XP_016863004.1:p.Glu43Val
|
|
XM_017007516.1:c.107A>T
|
XP_016863005.1:p.Glu36Val
|
|
NM_001106.4:c.110A>T
MANE Select
|
NP_001097.2:p.Glu37Val
|
|