ENST00000293404.8:c.1061C>T
(NAGS)
MANE Select
|
ENSP00000293404.2:p.Ala354Val
|
|
ENST00000293404.7:c.1061C>T
(NAGS)
|
ENSP00000293404.2:p.Ala354Val
|
|
ENST00000589767.1:c.968C>T
(NAGS)
|
ENSP00000465408.1:p.Ala323Val
|
|
ENST00000592915.1:n.336C>T
(NAGS)
|
|
|
NM_153006.2:c.1061C>T
(NAGS)
|
NP_694551.1:p.Ala354Val
|
|
XM_011524438.1:c.1061C>T
(NAGS)
|
XP_011522740.1:p.Ala354Val
|
|
XM_011524439.1:c.563C>T
(NAGS)
|
XP_011522741.1:p.Ala188Val
|
|
XM_011525035.1:c.-463+16898G>A
(PYY)
|
XP_011523337.1:n.-463+16898G>A
|
|
XM_011524439.2:c.563C>T
(NAGS)
|
XP_011522741.1:p.Ala188Val
|
|
NM_153006.3:c.1061C>T
(NAGS)
MANE Select
|
NP_694551.1:p.Ala354Val
|
|