ENST00000220616.9:c.8050C>G
MANE Select
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ENSP00000220616.4:p.Pro2684Ala
|
|
ENST00000220616.8:c.8050C>G
|
ENSP00000220616.4:p.Pro2684Ala
|
|
ENST00000519178.5:c.3416C>G
|
|
|
ENST00000519543.5:c.2449C>G
|
ENSP00000430430.1:p.Pro817Ala
|
|
ENST00000521107.1:c.262C>G
|
ENSP00000430161.1:p.Pro88Ala
|
|
ENST00000522691.1:n.136C>G
|
|
|
ENST00000523756.5:c.4705C>G
|
|
|
NM_003235.4:c.8050C>G
|
NP_003226.4:p.Pro2684Ala
|
|
XM_005251038.3:c.7858C>G
|
XP_005251095.1:p.Pro2620Ala
|
|
XM_006716622.2:c.7987C>G
|
XP_006716685.1:p.Pro2663Ala
|
|
XM_005251038.4:c.7858C>G
|
XP_005251095.1:p.Pro2620Ala
|
|
XM_006716622.3:c.7987C>G
|
XP_006716685.1:p.Pro2663Ala
|
|
XM_017013793.1:c.7984C>G
|
XP_016869282.1:p.Pro2662Ala
|
|
XM_017013794.1:c.7915C>G
|
XP_016869283.1:p.Pro2639Ala
|
|
XM_017013795.1:c.7879C>G
|
XP_016869284.1:p.Pro2627Ala
|
|
XM_017013796.1:c.7831C>G
|
XP_016869285.1:p.Pro2611Ala
|
|
XM_017013797.1:c.7789C>G
|
XP_016869286.1:p.Pro2597Ala
|
|
NM_003235.5:c.8050C>G
MANE Select
|
NP_003226.4:p.Pro2684Ala
|
|