ENST00000293404.8:c.846C>T
(NAGS)
MANE Select
|
ENSP00000293404.2:p.Ala282=
|
|
ENST00000293404.7:c.846C>T
(NAGS)
|
ENSP00000293404.2:p.Ala282=
|
|
ENST00000589767.1:c.753C>T
(NAGS)
|
ENSP00000465408.1:p.Ala251=
|
|
ENST00000592915.1:n.121C>T
(NAGS)
|
|
|
NM_153006.2:c.846C>T
(NAGS)
|
NP_694551.1:p.Ala282=
|
|
XM_011524438.1:c.846C>T
(NAGS)
|
XP_011522740.1:p.Ala282=
|
|
XM_011524439.1:c.348C>T
(NAGS)
|
XP_011522741.1:p.Ala116=
|
|
XM_011525035.1:c.-463+17404G>A
(PYY)
|
XP_011523337.1:n.-463+17404G>A
|
|
XM_011524439.2:c.348C>T
(NAGS)
|
XP_011522741.1:p.Ala116=
|
|
NM_153006.3:c.846C>T
(NAGS)
MANE Select
|
NP_694551.1:p.Ala282=
|
|