ENST00000430262.3:c.1048+46C>T
MANE Select
|
ENSP00000416305.2:n.1048+46C>T
|
|
ENST00000362063.6:c.1048+46C>T
|
ENSP00000354686.2:n.1048+46C>T
|
|
ENST00000430262.2:c.1048+46C>T
|
ENSP00000416305.2:n.1048+46C>T
|
|
ENST00000508237.5:c.508+46C>T
|
ENSP00000424848.1:n.508+46C>T
|
|
NM_001145365.1:c.1048+46C>T
|
NP_001138837.1:n.1048+46C>T
|
|
NM_014897.2:c.1048+46C>T
|
NP_055712.1:n.1048+46C>T
|
|
XM_005257166.1:c.508+46C>T
|
XP_005257223.1:n.508+46C>T
|
|
XR_934423.1:n.1259+46C>T
|
|
|
XR_934424.1:n.890+46C>T
|
|
|
NR_135579.1:n.1096+46C>T
|
|
|
XM_024450653.1:c.1048+46C>T
|
XP_024306421.1:n.1048+46C>T
|
|
XM_024450654.1:c.1048+46C>T
|
XP_024306422.1:n.1048+46C>T
|
|
XM_024450655.1:c.1048+46C>T
|
XP_024306423.1:n.1048+46C>T
|
|
XM_024450656.1:c.508+46C>T
|
XP_024306424.1:n.508+46C>T
|
|
XR_934423.2:n.1460+46C>T
|
|
|
NM_001145365.2:c.1048+46C>T
|
NP_001138837.1:n.1048+46C>T
|
|
NR_135579.2:n.1232+46C>T
|
|
|
NM_001145365.3:c.1048+46C>T
MANE Select
|
NP_001138837.1:n.1048+46C>T
|
|