|
ENST00000303354.11:c.4017A>T
(SCN9A)
|
ENSP00000304748.7:p.Gly1339=
|
|
|
ENST00000409435.6:c.4017A>T
(SCN9A)
|
ENSP00000386330.2:p.Gly1339=
|
|
|
ENST00000642356.2:c.4017A>T
(SCN9A)
MANE Select
|
ENSP00000495601.1:p.Gly1339=
|
|
|
ENST00000644316.1:c.3861A>T
(SCN9A)
|
ENSP00000493939.1:p.Gly1287=
|
|
|
ENST00000645907.1:c.3984A>T
(SCN9A)
|
ENSP00000495983.1:p.Gly1328=
|
|
|
ENST00000303354.10:c.4017A>T
(SCN9A)
|
ENSP00000304748.7:p.Gly1339=
|
|
|
ENST00000409435.5:c.4017A>T
(SCN9A)
|
ENSP00000386330.1:p.Gly1339=
|
|
|
ENST00000409672.5:c.3984A>T
(SCN9A)
|
ENSP00000386306.1:p.Gly1328=
|
|
|
NM_002977.3:c.3984A>T , LRG_369t1:c.3984A>T
(SCN9A)
|
NP_002968.1:p.Gly1328=
|
|
|
NR_110260.1:n.612-19315T>A
(SCN1A-AS1)
|
|
|
|
XM_005246757.1:c.4017A>T
(SCN9A)
|
XP_005246814.1:p.Gly1339=
|
|
|
XM_011511616.1:c.4017A>T
(SCN9A)
|
XP_011509918.1:p.Gly1339=
|
|
|
XM_011511617.1:c.4017A>T
(SCN9A)
|
XP_011509919.1:p.Gly1339=
|
|
|
XM_011511618.1:c.3984A>T
(SCN9A)
|
XP_011509920.1:p.Gly1328=
|
|
|
XM_011511619.1:c.4017A>T
(SCN9A)
|
XP_011509921.1:p.Gly1339=
|
|
|
NM_001365536.1:c.4017A>T
(SCN9A)
MANE Select
|
NP_001352465.1:p.Gly1339=
|
|
|
XM_011511616.3:c.4017A>T
(SCN9A)
|
XP_011509918.1:p.Gly1339=
|
|
|
XM_011511617.2:c.4017A>T
(SCN9A)
|
XP_011509919.1:p.Gly1339=
|
|
|
XM_011511618.2:c.3984A>T
(SCN9A)
|
XP_011509920.1:p.Gly1328=
|
|
|
XM_011511619.2:c.4017A>T
(SCN9A)
|
XP_011509921.1:p.Gly1339=
|
|
|
XM_017004668.1:c.3630A>T
(SCN9A)
|
XP_016860157.1:p.Gly1210=
|
|
|
XM_017004669.1:c.3273A>T
(SCN9A)
|
XP_016860158.1:p.Gly1091=
|
|
