ENST00000220616.9:c.8180C>A
MANE Select
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ENSP00000220616.4:p.Thr2727Lys
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|
ENST00000220616.8:c.8180C>A
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ENSP00000220616.4:p.Thr2727Lys
|
|
ENST00000519178.5:c.3546C>A
|
|
|
ENST00000519543.5:c.2579C>A
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ENSP00000430430.1:p.Thr860Lys
|
|
ENST00000521107.1:c.392C>A
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ENSP00000430161.1:p.Thr131Lys
|
|
ENST00000522691.1:n.266C>A
|
|
|
ENST00000523756.5:c.4835C>A
|
|
|
NM_003235.4:c.8180C>A
|
NP_003226.4:p.Thr2727Lys
|
|
XM_005251038.3:c.7988C>A
|
XP_005251095.1:p.Thr2663Lys
|
|
XM_006716622.2:c.8117C>A
|
XP_006716685.1:p.Thr2706Lys
|
|
XM_005251038.4:c.7988C>A
|
XP_005251095.1:p.Thr2663Lys
|
|
XM_006716622.3:c.8117C>A
|
XP_006716685.1:p.Thr2706Lys
|
|
XM_017013793.1:c.8114C>A
|
XP_016869282.1:p.Thr2705Lys
|
|
XM_017013794.1:c.8045C>A
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XP_016869283.1:p.Thr2682Lys
|
|
XM_017013795.1:c.8009C>A
|
XP_016869284.1:p.Thr2670Lys
|
|
XM_017013796.1:c.7961C>A
|
XP_016869285.1:p.Thr2654Lys
|
|
XM_017013797.1:c.7919C>A
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XP_016869286.1:p.Thr2640Lys
|
|
NM_003235.5:c.8180C>A
MANE Select
|
NP_003226.4:p.Thr2727Lys
|
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