NM_000320.3:c.106T=
MANE Select
|
NP_000311.2:p.Trp36=
|
ENST00000281243.10:c.106T=
MANE Select
|
ENSP00000281243.5:p.Trp36=
|
NM_000320.2:c.106T=
|
NP_000311.2:p.Trp36=
|
NM_001306140.1:c.105+2587T=
|
NP_001293069.1:n.105+2587T=
|
NM_001306140.2:c.105+2587T=
|
NP_001293069.1:n.105+2587T=
|
NR_156494.1:n.286T=
|
|
NR_156494.2:n.142T=
|
|
ENST00000281243.9:c.106T=
|
ENSP00000281243.5:p.Trp36=
|
ENST00000428702.6:c.105+2587T=
|
ENSP00000390944.2:n.105+2587T=
|
ENST00000505710.1:c.33T=
|
|
ENST00000507439.5:c.106T=
|
ENSP00000423227.1:p.Trp36=
|
ENST00000508623.5:c.106T=
|
ENSP00000426377.1:p.Trp36=
|
ENST00000513615.5:c.106T=
|
ENSP00000422759.1:p.Trp36=
|
ENST00000514300.1:c.*37T=
|
ENSP00000426039.1:n.*37T=
|
ENST00000706645.1:n.1153T=
|
|
XR_241677.1:n.269T=
|
|