ENST00000265104.5:c.8213A>G
MANE Select
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ENSP00000265104.4:p.Asp2738Gly
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ENST00000681290.1:c.8168A>G
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ENSP00000505288.1:p.Asp2723Gly
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|
ENST00000265104.4:c.8213A>G
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ENSP00000265104.4:p.Asp2738Gly
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NM_001369.2:c.8213A>G
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NP_001360.1:p.Asp2738Gly
|
|
XM_005248262.2:c.8168A>G
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XP_005248319.1:p.Asp2723Gly
|
|
XM_011513990.1:c.8213A>G
|
XP_011512292.1:p.Asp2738Gly
|
|
XR_925598.1:n.8420A>G
|
|
|
XM_005248262.3:c.8321A>G
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XP_005248319.2:p.Asp2774Gly
|
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XM_017009177.1:c.8321A>G
|
XP_016864666.1:p.Asp2774Gly
|
|
XM_017009178.1:c.7226A>G
|
XP_016864667.1:p.Asp2409Gly
|
|
XM_017009179.2:c.7226A>G
|
XP_016864668.1:p.Asp2409Gly
|
|
XM_017009180.1:c.8321A>G
|
XP_016864669.1:p.Asp2774Gly
|
|
XM_017009181.1:c.8321A>G
|
XP_016864670.1:p.Asp2774Gly
|
|
XM_017009182.1:c.8321A>G
|
XP_016864671.1:p.Asp2774Gly
|
|
XM_017009183.1:c.8321A>G
|
XP_016864672.1:p.Asp2774Gly
|
|
XM_017009184.1:c.8321A>G
|
XP_016864673.1:p.Asp2774Gly
|
|
XM_017009185.1:c.3410A>G
|
XP_016864674.1:p.Asp1137Gly
|
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XM_017009186.1:c.2963A>G
|
XP_016864675.1:p.Asp988Gly
|
|
XM_017009188.1:c.2300A>G
|
XP_016864677.1:p.Asp767Gly
|
|
XM_024454388.1:c.7226A>G
|
XP_024310156.1:p.Asp2409Gly
|
|
XM_024454389.1:c.6815A>G
|
XP_024310157.1:p.Asp2272Gly
|
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XR_001742034.1:n.8338A>G
|
|
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XR_001742035.1:n.8338A>G
|
|
|
NM_001369.3:c.8213A>G
MANE Select
|
NP_001360.1:p.Asp2738Gly
|
|