ENST00000263579.5:c.377-10A>T
MANE Select
|
ENSP00000263579.4:n.377-10A>T
|
|
ENST00000648516.1:c.98-10A>T
|
ENSP00000497684.1:n.98-10A>T
|
|
ENST00000263579.4:c.377-10A>T
|
ENSP00000263579.4:n.377-10A>T
|
|
NM_014026.4:c.377-10A>T
|
NP_054745.1:n.377-10A>T
|
|
XM_011542778.1:c.398-10A>T
|
XP_011541080.1:n.398-10A>T
|
|
XM_011542779.1:c.98-10A>T
|
XP_011541081.1:n.98-10A>T
|
|
XM_011542780.1:c.98-10A>T
|
XP_011541082.1:n.98-10A>T
|
|
NM_001350236.1:c.398-10A>T
|
NP_001337165.1:n.398-10A>T
|
|
NM_014026.5:c.377-10A>T
|
NP_054745.1:n.377-10A>T
|
|
NM_014026.6:c.377-10A>T
MANE Select
|
NP_054745.1:n.377-10A>T
|
|
NM_001350236.2:c.398-10A>T
|
NP_001337165.1:n.398-10A>T
|
|