ENST00000220616.9:c.8155T>G
MANE Select
|
ENSP00000220616.4:p.Ser2719Ala
|
|
ENST00000220616.8:c.8155T>G
|
ENSP00000220616.4:p.Ser2719Ala
|
|
ENST00000519178.5:c.3521T>G
|
|
|
ENST00000519543.5:c.2554T>G
|
ENSP00000430430.1:p.Ser852Ala
|
|
ENST00000521107.1:c.367T>G
|
ENSP00000430161.1:p.Ser123Ala
|
|
ENST00000522691.1:n.241T>G
|
|
|
ENST00000523756.5:c.4810T>G
|
|
|
NM_003235.4:c.8155T>G
|
NP_003226.4:p.Ser2719Ala
|
|
XM_005251038.3:c.7963T>G
|
XP_005251095.1:p.Ser2655Ala
|
|
XM_006716622.2:c.8092T>G
|
XP_006716685.1:p.Ser2698Ala
|
|
XM_005251038.4:c.7963T>G
|
XP_005251095.1:p.Ser2655Ala
|
|
XM_006716622.3:c.8092T>G
|
XP_006716685.1:p.Ser2698Ala
|
|
XM_017013793.1:c.8089T>G
|
XP_016869282.1:p.Ser2697Ala
|
|
XM_017013794.1:c.8020T>G
|
XP_016869283.1:p.Ser2674Ala
|
|
XM_017013795.1:c.7984T>G
|
XP_016869284.1:p.Ser2662Ala
|
|
XM_017013796.1:c.7936T>G
|
XP_016869285.1:p.Ser2646Ala
|
|
XM_017013797.1:c.7894T>G
|
XP_016869286.1:p.Ser2632Ala
|
|
NM_003235.5:c.8155T>G
MANE Select
|
NP_003226.4:p.Ser2719Ala
|
|