ENST00000220616.9:c.8188G=
MANE Select
|
ENSP00000220616.4:p.Asp2730=
|
|
ENST00000220616.8:c.8188G=
|
ENSP00000220616.4:p.Asp2730=
|
|
ENST00000519178.5:c.3554G=
|
|
|
ENST00000519543.5:c.2587G=
|
ENSP00000430430.1:p.Asp863=
|
|
ENST00000521107.1:c.400G=
|
ENSP00000430161.1:p.Asp134=
|
|
ENST00000522691.1:n.274G=
|
|
|
ENST00000523756.5:c.4843G=
|
|
|
NM_003235.4:c.8188G=
|
NP_003226.4:p.Asp2730=
|
|
XM_005251038.3:c.7996G=
|
XP_005251095.1:p.Asp2666=
|
|
XM_006716622.2:c.8125G=
|
XP_006716685.1:p.Asp2709=
|
|
XM_005251038.4:c.7996G=
|
XP_005251095.1:p.Asp2666=
|
|
XM_006716622.3:c.8125G=
|
XP_006716685.1:p.Asp2709=
|
|
XM_017013793.1:c.8122G=
|
XP_016869282.1:p.Asp2708=
|
|
XM_017013794.1:c.8053G=
|
XP_016869283.1:p.Asp2685=
|
|
XM_017013795.1:c.8017G=
|
XP_016869284.1:p.Asp2673=
|
|
XM_017013796.1:c.7969G=
|
XP_016869285.1:p.Asp2657=
|
|
XM_017013797.1:c.7927G=
|
XP_016869286.1:p.Asp2643=
|
|
NM_003235.5:c.8188G=
MANE Select
|
NP_003226.4:p.Asp2730=
|
|