|
NM_181426.2:c.112A>T
MANE Select
|
NP_852091.1:p.Arg38Ter
|
|
ENST00000476379.6:c.112A>T
MANE Select
|
ENSP00000417960.2:p.Arg38Ter
|
|
NM_181426.1:c.112A>T
|
NP_852091.1:p.Arg38Ter
|
|
ENST00000442201.6:c.112A>T
|
ENSP00000405708.2:p.Arg38Ter
|
|
ENST00000471307.6:c.58A>T
|
ENSP00000418702.2:p.Arg20Ter
|
|
ENST00000476379.5:c.112A>T
|
ENSP00000417960.1:p.Arg38Ter
|
|
ENST00000650641.1:n.191A>T
|
|
|
ENST00000650889.1:n.284A>T
|
|
|
ENST00000651046.1:c.112A>T
|
ENSP00000499175.1:p.Arg38Ter
|
|
ENST00000651818.1:n.254A>T
|
|
|
ENST00000652024.1:n.203A>T
|
|
|
ENST00000652408.1:n.249A>T
|
|