ENST00000460843.6:c.2618G>A
MANE Select
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ENSP00000417980.1:p.Gly873Asp
|
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ENST00000636027.1:c.2504G>A
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ENSP00000489961.1:p.Gly835Asp
|
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ENST00000637161.1:c.2525G>A
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ENSP00000490328.1:p.Gly842Asp
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ENST00000637261.1:c.2658G>A
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ENSP00000490815.1:n.2658G>A
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ENST00000637891.1:c.512G>A
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ENSP00000490907.1:p.Gly171Asp
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ENST00000637949.1:c.296G>A
|
ENSP00000489786.1:p.Gly99Asp
|
|
ENST00000460843.5:c.2618G>A
|
ENSP00000417980.1:p.Gly873Asp
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|
ENST00000462942.3:c.1475G>A
|
ENSP00000436107.1:p.Gly492Asp
|
|
ENST00000482340.5:c.188G>A
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ENSP00000486748.1:p.Gly63Asp
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ENST00000486164.5:c.196G>A
|
|
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ENST00000488242.2:n.144G>A
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|
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ENST00000493484.5:c.188G>A
|
ENSP00000486503.1:p.Gly63Asp
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|
NM_024757.4:c.2618G>A
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NP_079033.4:p.Gly873Asp
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|
XM_005266105.3:c.2609G>A
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XP_005266162.1:p.Gly870Asp
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|
XM_005266110.1:c.2525G>A
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XP_005266167.1:p.Gly842Asp
|
|
XM_006717288.2:c.2600G>A
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XP_006717351.1:p.Gly867Asp
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XM_011519021.1:c.2627G>A
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XP_011517323.1:p.Gly876Asp
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|
XM_011519022.1:c.2624G>A
|
XP_011517324.1:p.Gly875Asp
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XM_011519023.1:c.2606G>A
|
XP_011517325.1:p.Gly869Asp
|
|
XM_011519024.1:c.2549G>A
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XP_011517326.1:p.Gly850Asp
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|
XM_011519025.1:c.2525G>A
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XP_011517327.1:p.Gly842Asp
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|
XM_011519026.1:c.2483G>A
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XP_011517328.1:p.Gly828Asp
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|
XM_011519027.1:c.2627G>A
|
XP_011517329.1:p.Gly876Asp
|
|
XM_011519029.1:c.1049G>A
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XP_011517331.1:p.Gly350Asp
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|
XM_011519030.1:c.401G>A
|
XP_011517332.1:p.Gly134Asp
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|
XM_011519031.1:c.188G>A
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XP_011517333.1:p.Gly63Asp
|
|
XM_011519032.1:c.188G>A
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XP_011517334.1:p.Gly63Asp
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|
XM_011519033.1:c.2462G>A
|
XP_011517335.1:p.Gly821Asp
|
|
NM_001354263.1:c.2597G>A
|
NP_001341192.1:p.Gly866Asp
|
|
XM_005266105.5:c.2609G>A
|
XP_005266162.1:p.Gly870Asp
|
|
XM_011519021.3:c.2627G>A
|
XP_011517323.1:p.Gly876Asp
|
|
XM_011519022.3:c.2624G>A
|
XP_011517324.1:p.Gly875Asp
|
|
XM_011519023.3:c.2606G>A
|
XP_011517325.1:p.Gly869Asp
|
|
XM_011519029.3:c.1049G>A
|
XP_011517331.1:p.Gly350Asp
|
|
XM_011519030.3:c.401G>A
|
XP_011517332.1:p.Gly134Asp
|
|
XM_017015134.1:c.2603G>A
|
XP_016870623.1:p.Gly868Asp
|
|
XM_017015136.2:c.2519G>A
|
XP_016870625.1:p.Gly840Asp
|
|
XM_017015137.1:c.2504G>A
|
XP_016870626.1:p.Gly835Asp
|
|
XM_017015138.1:c.2504G>A
|
XP_016870627.1:p.Gly835Asp
|
|
XM_024447674.1:c.2447G>A
|
XP_024303442.1:p.Gly816Asp
|
|
XM_024447675.1:c.2381G>A
|
XP_024303443.1:p.Gly794Asp
|
|
XM_024447676.1:c.1742G>A
|
XP_024303444.1:p.Gly581Asp
|
|
XM_024447677.1:c.1742G>A
|
XP_024303445.1:p.Gly581Asp
|
|
XM_024447678.1:c.2525G>A
|
XP_024303446.1:p.Gly842Asp
|
|
XM_024447680.1:c.2360G>A
|
XP_024303448.1:p.Gly787Asp
|
|
NM_024757.5:c.2618G>A
MANE Select
|
NP_079033.4:p.Gly873Asp
|
|
NM_001354263.2:c.2597G>A
|
NP_001341192.1:p.Gly866Asp
|
|