ENST00000263579.5:c.902T=
(DCPS)
MANE Select
|
ENSP00000263579.4:p.Val301=
|
|
ENST00000648516.1:c.623T=
(DCPS)
|
ENSP00000497684.1:p.Val208=
|
|
ENST00000263579.4:c.902T=
(DCPS)
|
ENSP00000263579.4:p.Val301=
|
|
ENST00000529149.1:n.2252T=
(DCPS)
|
|
|
ENST00000530860.5:n.413T=
(DCPS)
|
|
|
NM_014026.4:c.902T=
(DCPS)
|
NP_054745.1:p.Val301=
|
|
NR_033839.1:n.147-3179A=
(GSEC)
|
|
|
XM_011542778.1:c.923T=
(DCPS)
|
XP_011541080.1:p.Val308=
|
|
XM_011542779.1:c.623T=
(DCPS)
|
XP_011541081.1:p.Val208=
|
|
XM_011542780.1:c.623T=
(DCPS)
|
XP_011541082.1:p.Val208=
|
|
NM_001350236.1:c.923T=
(DCPS)
|
NP_001337165.1:p.Val308=
|
|
NM_014026.5:c.902T=
(DCPS)
|
NP_054745.1:p.Val301=
|
|
NM_014026.6:c.902T=
(DCPS)
MANE Select
|
NP_054745.1:p.Val301=
|
|
NM_001350236.2:c.923T=
(DCPS)
|
NP_001337165.1:p.Val308=
|
|