ENST00000220616.9:c.8121A>T
MANE Select
|
ENSP00000220616.4:p.Arg2707=
|
|
ENST00000220616.8:c.8121A>T
|
ENSP00000220616.4:p.Arg2707=
|
|
ENST00000519178.5:c.3487A>T
|
|
|
ENST00000519543.5:c.2520A>T
|
ENSP00000430430.1:p.Arg840=
|
|
ENST00000521107.1:c.333A>T
|
ENSP00000430161.1:p.Arg111=
|
|
ENST00000522691.1:n.207A>T
|
|
|
ENST00000523756.5:c.4776A>T
|
|
|
NM_003235.4:c.8121A>T
|
NP_003226.4:p.Arg2707=
|
|
XM_005251038.3:c.7929A>T
|
XP_005251095.1:p.Arg2643=
|
|
XM_006716622.2:c.8058A>T
|
XP_006716685.1:p.Arg2686=
|
|
XM_005251038.4:c.7929A>T
|
XP_005251095.1:p.Arg2643=
|
|
XM_006716622.3:c.8058A>T
|
XP_006716685.1:p.Arg2686=
|
|
XM_017013793.1:c.8055A>T
|
XP_016869282.1:p.Arg2685=
|
|
XM_017013794.1:c.7986A>T
|
XP_016869283.1:p.Arg2662=
|
|
XM_017013795.1:c.7950A>T
|
XP_016869284.1:p.Arg2650=
|
|
XM_017013796.1:c.7902A>T
|
XP_016869285.1:p.Arg2634=
|
|
XM_017013797.1:c.7860A>T
|
XP_016869286.1:p.Arg2620=
|
|
NM_003235.5:c.8121A>T
MANE Select
|
NP_003226.4:p.Arg2707=
|
|