ENST00000399391.7:c.482A>T
|
ENSP00000382323.2:p.Glu161Val
|
|
ENST00000399397.6:c.446A>T
MANE Select
|
ENSP00000382329.2:p.Glu149Val
|
|
ENST00000399391.6:c.482A>T
|
ENSP00000382323.2:p.Glu161Val
|
|
ENST00000399397.5:c.446A>T
|
ENSP00000382329.2:p.Glu149Val
|
|
ENST00000428619.1:c.263A>T
|
ENSP00000399057.2:p.Glu88Val
|
|
ENST00000498332.5:n.352A>T
|
|
|
NM_001277269.1:c.482A>T
|
NP_001264198.1:p.Glu161Val
|
|
NM_001292063.1:c.446A>T
|
NP_001278992.1:p.Glu149Val
|
|
NM_001277269.2:c.482A>T
|
NP_001264198.1:p.Glu161Val
|
|
NM_001292063.2:c.446A>T
MANE Select
|
NP_001278992.1:p.Glu149Val
|
|