ENST00000331456.7:c.725A>T
MANE Select
|
ENSP00000328203.2:p.Glu242Val
|
|
ENST00000331456.6:c.725A>T
|
ENSP00000328203.2:p.Glu242Val
|
|
ENST00000469027.5:c.260A>T
|
ENSP00000420085.1:p.Glu87Val
|
|
ENST00000473195.5:c.300A>T
|
ENSP00000419556.1:p.Ter100Cys
|
|
ENST00000475495.1:n.199A>T
|
|
|
ENST00000482582.5:c.677A>T
|
ENSP00000418544.1:p.Glu226Val
|
|
NM_005879.2:c.725A>T
|
NP_005870.2:p.Glu242Val
|
|
XM_011533264.1:c.494A>T
|
XP_011531566.1:p.Glu165Val
|
|
XR_940361.1:n.835A>T
|
|
|
XM_017005526.1:c.428A>T
|
XP_016861015.1:p.Glu143Val
|
|
XR_001739979.1:n.835A>T
|
|
|
NM_005879.3:c.725A>T
MANE Select
|
NP_005870.2:p.Glu242Val
|
|