ENST00000320580.9:c.608G=
MANE Select
|
ENSP00000316454.4:p.Arg203=
|
|
ENST00000320580.8:c.608G=
|
ENSP00000316454.4:p.Arg203=
|
|
ENST00000527224.1:n.732G=
|
|
|
ENST00000527380.1:c.314G=
|
ENSP00000432639.1:p.Arg105=
|
|
ENST00000533756.5:c.299G=
|
ENSP00000437150.1:p.Arg100=
|
|
NM_018026.3:c.608G=
|
NP_060496.2:p.Arg203=
|
|
XM_011545162.1:c.287G=
|
XP_011543464.1:p.Arg96=
|
|
XM_011545163.1:c.278G=
|
XP_011543465.1:p.Arg93=
|
|
XM_011545164.1:c.269G=
|
XP_011543466.1:p.Arg90=
|
|
XM_011545164.2:c.269G=
|
XP_011543466.1:p.Arg90=
|
|
XR_001747924.1:n.819G=
|
|
|
NM_018026.4:c.608G=
MANE Select
|
NP_060496.2:p.Arg203=
|
|