|
ENST00000270235.11:c.651C>T
(NTN5)
MANE Select
|
ENSP00000270235.4:p.His217=
|
|
|
ENST00000270235.8:c.651C>T
(NTN5)
|
ENSP00000270235.3:p.His217=
|
|
|
ENST00000430145.3:n.119+1481G>A
(SEC1P)
|
|
|
|
ENST00000474419.5:n.147+1481G>A
(SEC1P)
|
|
|
|
ENST00000483163.1:n.77-15277G>A
(SEC1P)
|
|
|
|
ENST00000596844.5:c.-307C>T
(NTN5)
|
ENSP00000469490.1:n.-307C>T
|
|
|
ENST00000600468.1:n.767C>T
(NTN5)
|
|
|
|
NM_145807.2:c.651C>T
(NTN5)
|
NP_665806.1:p.His217=
|
|
|
NR_004401.2:n.179+1481G>A
(SEC1P)
|
|
|
|
XM_011526443.1:c.651C>T
(NTN5)
|
XP_011524745.1:p.His217=
|
|
|
XM_011526443.3:c.651C>T
(NTN5)
|
XP_011524745.1:p.His217=
|
|
|
XM_017026274.1:c.186C>T
(NTN5)
|
XP_016881763.1:p.His62=
|
|
|
NM_145807.3:c.651C>T
(NTN5)
|
NP_665806.1:p.His217=
|
|
|
NM_145807.4:c.651C>T
(NTN5)
MANE Select
|
NP_665806.1:p.His217=
|
|
