|
ENST00000465370.2:c.2106G>T
(NSF)
|
ENSP00000467779.2:p.Lys702Asn
|
|
|
ENST00000571864.6:c.*1820G>T
(NSF)
|
ENSP00000461448.1:n.*1820G>T
|
|
|
ENST00000576040.6:c.2091G>T
(NSF)
|
ENSP00000460152.2:p.Lys697Asn
|
|
|
ENST00000576346.6:n.692G>T
(NSF)
|
|
|
|
ENST00000706373.1:c.2106G>T
(NSF)
|
ENSP00000516356.1:p.Lys702Asn
|
|
|
ENST00000706374.1:n.2188G>T
(NSF)
|
|
|
|
ENST00000706391.1:c.2106G>T
(NSF)
|
ENSP00000516368.1:p.Lys702Asn
|
|
|
ENST00000706392.1:c.2106G>T
(NSF)
|
ENSP00000516369.1:p.Lys702Asn
|
|
|
ENST00000706393.1:c.2106G>T
(NSF)
|
ENSP00000516370.1:p.Lys702Asn
|
|
|
ENST00000706395.1:c.1719G>T
(NSF)
|
ENSP00000516371.1:p.Lys573Asn
|
|
|
ENST00000706396.1:c.1815G>T
(NSF)
|
ENSP00000516372.1:p.Lys605Asn
|
|
|
ENST00000706397.1:c.*639G>T
(NSF)
|
ENSP00000516373.1:n.*639G>T
|
|
|
ENST00000706398.1:c.1668G>T
(NSF)
|
ENSP00000516374.1:p.Lys556Asn
|
|
|
ENST00000706399.1:c.1824G>T
(NSF)
|
ENSP00000516375.1:p.Lys608Asn
|
|
|
ENST00000706400.1:c.2091G>T
(NSF)
|
ENSP00000516376.1:p.Lys697Asn
|
|
|
ENST00000706401.1:c.*1849G>T
(NSF)
|
ENSP00000516377.1:n.*1849G>T
|
|
|
ENST00000706403.1:n.1428G>T
(NSF)
|
|
|
|
ENST00000706405.1:n.1277G>T
(NSF)
|
|
|
|
ENST00000398238.8:c.2106G>T
(NSF)
MANE Select
|
ENSP00000381293.4:p.Lys702Asn
|
|
|
ENST00000465370.1:c.338G>T
(NSF)
|
|
|
|
ENST00000575068.5:c.2091G>T
(NSF)
|
ENSP00000458221.1:p.Lys697Asn
|
|
|
ENST00000576346.5:c.390G>T
(NSF)
|
ENSP00000459646.1:p.Lys130Asn
|
|
|
NM_006178.3:c.2106G>T
(NSF)
|
NP_006169.2:p.Lys702Asn
|
|
|
NR_040116.1:n.2173G>T
(NSF)
|
|
|
|
XM_011524863.1:c.2106G>T
(NSF)
|
XP_011523165.1:p.Lys702Asn
|
|
|
XM_024450773.1:c.4809+201046G>T
(LRRC37A2)
|
XP_024306541.1:n.4809+201046G>T
|
|
|
NM_006178.4:c.2106G>T
(NSF)
MANE Select
|
NP_006169.2:p.Lys702Asn
|
|
|
NR_040116.2:n.2173G>T
(NSF)
|
|
|
