ENST00000291536.8:c.730G>A
MANE Select
|
ENSP00000291536.3:p.Ala244Thr
|
|
ENST00000291536.7:c.730G>A
|
ENSP00000291536.3:p.Ala244Thr
|
|
ENST00000398352.3:c.616G>A
|
ENSP00000381395.3:p.Ala206Thr
|
|
ENST00000493019.1:n.2348G>A
|
|
|
NM_001286506.1:c.616G>A
|
NP_001273435.1:p.Ala206Thr
|
|
NM_080860.3:c.730G>A
|
NP_543136.1:p.Ala244Thr
|
|
XM_005261208.1:c.523G>A
|
XP_005261265.1:p.Ala175Thr
|
|
XM_011529786.1:c.658G>A
|
XP_011528088.1:p.Ala220Thr
|
|
XM_005261208.2:c.523G>A
|
XP_005261265.1:p.Ala175Thr
|
|
NM_080860.4:c.730G>A
MANE Select
|
NP_543136.1:p.Ala244Thr
|
|
NM_001286506.2:c.616G>A
|
NP_001273435.1:p.Ala206Thr
|
|