ENST00000293404.8:c.1430T>A
(NAGS)
MANE Select
|
ENSP00000293404.2:p.Val477Asp
|
|
ENST00000293404.7:c.1430T>A
(NAGS)
|
ENSP00000293404.2:p.Val477Asp
|
|
ENST00000589767.1:c.1361T>A
(NAGS)
|
ENSP00000465408.1:p.Val454Asp
|
|
ENST00000592915.1:n.1318T>A
(NAGS)
|
|
|
NM_153006.2:c.1430T>A
(NAGS)
|
NP_694551.1:p.Val477Asp
|
|
XM_011524438.1:c.1268+258T>A
(NAGS)
|
XP_011522740.1:n.1268+258T>A
|
|
XM_011524439.1:c.932T>A
(NAGS)
|
XP_011522741.1:p.Val311Asp
|
|
XM_011525035.1:c.-463+15820A>T
(PYY)
|
XP_011523337.1:n.-463+15820A>T
|
|
XM_011524439.2:c.932T>A
(NAGS)
|
XP_011522741.1:p.Val311Asp
|
|
NM_153006.3:c.1430T>A
(NAGS)
MANE Select
|
NP_694551.1:p.Val477Asp
|
|