|
NM_000079.4:c.1143C>T
MANE Select
|
NP_000070.1:p.Gly381=
|
|
ENST00000348749.9:c.1143C>T
MANE Select
|
ENSP00000261008.5:p.Gly381=
|
|
NM_000079.3:c.1143C>T
|
NP_000070.1:p.Gly381=
|
|
NM_001039523.2:c.1218C>T
|
NP_001034612.1:p.Gly406=
|
|
NM_001039523.3:c.1218C>T
|
NP_001034612.1:p.Gly406=
|
|
ENST00000261007.9:c.1218C>T
|
ENSP00000261007.5:p.Gly406=
|
|
ENST00000409219.5:c.1003-424C>T
|
ENSP00000386611.1:n.1003-424C>T
|
|
ENST00000409542.5:c.897C>T
|
ENSP00000387026.1:p.Gly299=
|
|
ENST00000435083.5:c.*787C>T
|
ENSP00000395805.1:n.*787C>T
|
|
ENST00000636168.2:c.654C>T
|
ENSP00000490338.2:p.Gly218=
|
|
ENST00000672640.1:c.654C>T
|
ENSP00000500507.1:p.Gly218=
|
|
XM_017003256.1:c.1239C>T
|
XP_016858745.1:p.Gly413=
|
|
XM_017003257.1:c.1164C>T
|
XP_016858746.1:p.Gly388=
|