ENST00000220616.9:c.8084A>G
MANE Select
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ENSP00000220616.4:p.Glu2695Gly
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ENST00000220616.8:c.8084A>G
|
ENSP00000220616.4:p.Glu2695Gly
|
|
ENST00000519178.5:c.3450A>G
|
|
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ENST00000519543.5:c.2483A>G
|
ENSP00000430430.1:p.Glu828Gly
|
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ENST00000521107.1:c.296A>G
|
ENSP00000430161.1:p.Glu99Gly
|
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ENST00000522691.1:n.170A>G
|
|
|
ENST00000523756.5:c.4739A>G
|
|
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NM_003235.4:c.8084A>G
|
NP_003226.4:p.Glu2695Gly
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XM_005251038.3:c.7892A>G
|
XP_005251095.1:p.Glu2631Gly
|
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XM_006716622.2:c.8021A>G
|
XP_006716685.1:p.Glu2674Gly
|
|
XM_005251038.4:c.7892A>G
|
XP_005251095.1:p.Glu2631Gly
|
|
XM_006716622.3:c.8021A>G
|
XP_006716685.1:p.Glu2674Gly
|
|
XM_017013793.1:c.8018A>G
|
XP_016869282.1:p.Glu2673Gly
|
|
XM_017013794.1:c.7949A>G
|
XP_016869283.1:p.Glu2650Gly
|
|
XM_017013795.1:c.7913A>G
|
XP_016869284.1:p.Glu2638Gly
|
|
XM_017013796.1:c.7865A>G
|
XP_016869285.1:p.Glu2622Gly
|
|
XM_017013797.1:c.7823A>G
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XP_016869286.1:p.Glu2608Gly
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|
NM_003235.5:c.8084A>G
MANE Select
|
NP_003226.4:p.Glu2695Gly
|
|