ENST00000399820.8:c.2597G>C
MANE Select
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ENSP00000382717.3:p.Gly866Ala
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ENST00000399820.7:c.2597G>C
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ENSP00000382717.3:p.Gly866Ala
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ENST00000506869.5:c.*2178G>C
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ENSP00000424319.1:n.*2178G>C
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ENST00000512095.5:n.1595G>C
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|
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NM_025132.3:c.2597G>C
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NP_079408.3:p.Gly866Ala
|
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XM_011513724.1:c.2609G>C
|
XP_011512026.1:p.Gly870Ala
|
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XM_011513725.1:c.2543G>C
|
XP_011512027.1:p.Gly848Ala
|
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XM_011513726.1:c.2129G>C
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XP_011512028.1:p.Gly710Ala
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XM_011513727.1:c.2129G>C
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XP_011512029.1:p.Gly710Ala
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XM_011513728.1:c.2117G>C
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XP_011512030.1:p.Gly706Ala
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|
XM_011513729.1:c.2609G>C
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XP_011512031.1:p.Gly870Ala
|
|
XR_925155.1:n.2673G>C
|
|
|
NM_001317924.1:c.2117G>C
|
NP_001304853.1:p.Gly706Ala
|
|
XM_011513725.2:c.2543G>C
|
XP_011512027.1:p.Gly848Ala
|
|
XM_011513726.3:c.2129G>C
|
XP_011512028.1:p.Gly710Ala
|
|
XM_017008501.1:c.2117G>C
|
XP_016863990.1:p.Gly706Ala
|
|
XR_001741306.1:n.2673G>C
|
|
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XR_001741307.1:n.2661G>C
|
|
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XR_001741308.1:n.2673G>C
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XR_001741309.1:n.2661G>C
|
|
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XR_001741310.1:n.2661G>C
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|
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XR_001741311.2:n.2510G>C
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|
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NM_025132.4:c.2597G>C
MANE Select
|
NP_079408.3:p.Gly866Ala
|
|
NM_001317924.2:c.2117G>C
|
NP_001304853.1:p.Gly706Ala
|
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