|
NM_000343.4:c.799C>T
MANE Select
|
NP_000334.1:p.Arg267Ter
|
|
ENST00000266088.9:c.799C>T
MANE Select
|
ENSP00000266088.4:p.Arg267Ter
|
|
NM_000343.3:c.799C>T
|
NP_000334.1:p.Arg267Ter
|
|
NM_001256314.1:c.418C>T
|
NP_001243243.1:p.Arg140Ter
|
|
NM_001256314.2:c.418C>T
|
NP_001243243.1:p.Arg140Ter
|
|
ENST00000266088.8:c.799C>T
|
ENSP00000266088.4:p.Arg267Ter
|
|
ENST00000486394.1:n.239C>T
|
|
|
ENST00000543737.2:c.418C>T
|
ENSP00000444898.1:p.Arg140Ter
|
|
XM_011530331.1:c.799C>T
|
XP_011528633.1:p.Arg267Ter
|
|
XR_938173.1:n.592-15770G>A
|
|
|
XR_938174.1:n.487-15770G>A
|
|