ENST00000682775.1:c.2186-12254A>T
(SACS)
|
ENSP00000508399.1:n.2186-12254A>T
|
|
ENST00000683210.1:c.2185+29416A>T
(SACS)
|
ENSP00000506739.1:n.2185+29416A>T
|
|
ENST00000684325.1:c.2186-2695A>T
(SACS)
|
ENSP00000508121.1:n.2186-2695A>T
|
|
ENST00000684497.1:c.2186-1725A>T
(SACS)
|
ENSP00000507057.1:n.2186-1725A>T
|
|
ENST00000218867.4:c.704T>A
(SGCG)
MANE Select
|
ENSP00000218867.3:p.Leu235His
|
|
ENST00000218867.3:c.704T>A
(SGCG)
|
ENSP00000218867.3:p.Leu235His
|
|
NM_000231.2:c.704T>A , LRG_207t1:c.704T>A
(SGCG)
|
NP_000222.1:p.Leu235His
|
|
XM_005266505.2:c.704T>A
(SGCG)
|
XP_005266562.1:p.Leu235His
|
|
XM_006719861.2:c.758T>A
(SGCG)
|
XP_006719924.1:p.Leu253His
|
|
XM_006719861.3:c.758T>A
(SGCG)
|
XP_006719924.1:p.Leu253His
|
|
XM_024449397.1:c.704T>A
(SGCG)
|
XP_024305165.1:p.Leu235His
|
|
NM_000231.3:c.704T>A
(SGCG)
MANE Select
|
NP_000222.2:p.Leu235His
|
|
NM_001378244.1:c.758T>A
(SGCG)
|
NP_001365173.1:p.Leu253His
|
|
NM_001378245.1:c.704T>A
(SGCG)
|
NP_001365174.1:p.Leu235His
|
|
NM_001378246.1:c.704T>A
(SGCG)
|
NP_001365175.1:p.Leu235His
|
|