|
ENST00000303354.11:c.1232C>T
(SCN9A)
|
ENSP00000304748.7:p.Ala411Val
|
|
|
ENST00000409435.6:c.1232C>T
(SCN9A)
|
ENSP00000386330.2:p.Ala411Val
|
|
|
ENST00000454569.6:c.1232C>T
(SCN9A)
|
ENSP00000413212.2:p.Ala411Val
|
|
|
ENST00000642356.2:c.1232C>T
(SCN9A)
MANE Select
|
ENSP00000495601.1:p.Ala411Val
|
|
|
ENST00000644316.1:c.1232C>T
(SCN9A)
|
ENSP00000493939.1:p.Ala411Val
|
|
|
ENST00000645907.1:c.1232C>T
(SCN9A)
|
ENSP00000495983.1:p.Ala411Val
|
|
|
ENST00000667201.2:c.267C>T
(SCN9A)
|
|
|
|
ENST00000303354.10:c.1232C>T
(SCN9A)
|
ENSP00000304748.7:p.Ala411Val
|
|
|
ENST00000409435.5:c.1232C>T
(SCN9A)
|
ENSP00000386330.1:p.Ala411Val
|
|
|
ENST00000409672.5:c.1232C>T
(SCN9A)
|
ENSP00000386306.1:p.Ala411Val
|
|
|
ENST00000452182.1:c.827C>T
(SCN9A)
|
ENSP00000393141.1:p.Ala276Val
|
|
|
ENST00000454569.5:c.827C>T
(SCN9A)
|
ENSP00000413212.1:p.Ala276Val
|
|
|
NM_002977.3:c.1232C>T , LRG_369t1:c.1232C>T
(SCN9A)
|
NP_002968.1:p.Ala411Val
|
|
|
NR_110260.1:n.1030-6046G>A
(SCN1A-AS1)
|
|
|
|
XM_005246757.1:c.1232C>T
(SCN9A)
|
XP_005246814.1:p.Ala411Val
|
|
|
XM_011511616.1:c.1232C>T
(SCN9A)
|
XP_011509918.1:p.Ala411Val
|
|
|
XM_011511617.1:c.1232C>T
(SCN9A)
|
XP_011509919.1:p.Ala411Val
|
|
|
XM_011511618.1:c.1232C>T
(SCN9A)
|
XP_011509920.1:p.Ala411Val
|
|
|
XM_011511619.1:c.1232C>T
(SCN9A)
|
XP_011509921.1:p.Ala411Val
|
|
|
NM_001365536.1:c.1232C>T
(SCN9A)
MANE Select
|
NP_001352465.1:p.Ala411Val
|
|
|
XM_011511616.3:c.1232C>T
(SCN9A)
|
XP_011509918.1:p.Ala411Val
|
|
|
XM_011511617.2:c.1232C>T
(SCN9A)
|
XP_011509919.1:p.Ala411Val
|
|
|
XM_011511618.2:c.1232C>T
(SCN9A)
|
XP_011509920.1:p.Ala411Val
|
|
|
XM_011511619.2:c.1232C>T
(SCN9A)
|
XP_011509921.1:p.Ala411Val
|
|
|
XM_017004668.1:c.845C>T
(SCN9A)
|
XP_016860157.1:p.Ala282Val
|
|
|
XM_017004669.1:c.488C>T
(SCN9A)
|
XP_016860158.1:p.Ala163Val
|
|
|
XR_001738886.1:n.1546C>T
(SCN9A)
|
|
|
