ENST00000263579.5:c.936C>G
(DCPS)
MANE Select
|
ENSP00000263579.4:p.Tyr312Ter
|
|
ENST00000648516.1:c.657C>G
(DCPS)
|
ENSP00000497684.1:p.Tyr219Ter
|
|
ENST00000263579.4:c.936C>G
(DCPS)
|
ENSP00000263579.4:p.Tyr312Ter
|
|
ENST00000529149.1:n.2286C>G
(DCPS)
|
|
|
ENST00000530860.5:n.447C>G
(DCPS)
|
|
|
NM_014026.4:c.936C>G
(DCPS)
|
NP_054745.1:p.Tyr312Ter
|
|
NR_033839.1:n.147-3213G>C
(GSEC)
|
|
|
XM_011542778.1:c.957C>G
(DCPS)
|
XP_011541080.1:p.Tyr319Ter
|
|
XM_011542779.1:c.657C>G
(DCPS)
|
XP_011541081.1:p.Tyr219Ter
|
|
XM_011542780.1:c.657C>G
(DCPS)
|
XP_011541082.1:p.Tyr219Ter
|
|
NM_001350236.1:c.957C>G
(DCPS)
|
NP_001337165.1:p.Tyr319Ter
|
|
NM_014026.5:c.936C>G
(DCPS)
|
NP_054745.1:p.Tyr312Ter
|
|
NM_014026.6:c.936C>G
(DCPS)
MANE Select
|
NP_054745.1:p.Tyr312Ter
|
|
NM_001350236.2:c.957C>G
(DCPS)
|
NP_001337165.1:p.Tyr319Ter
|
|