ENST00000683611.1:n.1138A>G
|
|
|
ENST00000265104.5:c.13805A>G
MANE Select
|
ENSP00000265104.4:p.Asp4602Gly
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ENST00000681290.1:c.13760A>G
|
ENSP00000505288.1:p.Asp4587Gly
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|
ENST00000265104.4:c.13805A>G
|
ENSP00000265104.4:p.Asp4602Gly
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NM_001369.2:c.13805A>G
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NP_001360.1:p.Asp4602Gly
|
|
XM_005248262.2:c.13760A>G
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XP_005248319.1:p.Asp4587Gly
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XM_005248262.3:c.13913A>G
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XP_005248319.2:p.Asp4638Gly
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XM_017009177.1:c.13493A>G
|
XP_016864666.1:p.Asp4498Gly
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XM_017009178.1:c.12818A>G
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XP_016864667.1:p.Asp4273Gly
|
|
XM_017009179.2:c.12818A>G
|
XP_016864668.1:p.Asp4273Gly
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|
XM_017009185.1:c.9002A>G
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XP_016864674.1:p.Asp3001Gly
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XM_017009186.1:c.8555A>G
|
XP_016864675.1:p.Asp2852Gly
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|
XM_017009188.1:c.7892A>G
|
XP_016864677.1:p.Asp2631Gly
|
|
XM_024454388.1:c.12818A>G
|
XP_024310156.1:p.Asp4273Gly
|
|
XM_024454389.1:c.12407A>G
|
XP_024310157.1:p.Asp4136Gly
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|
NM_001369.3:c.13805A>G
MANE Select
|
NP_001360.1:p.Asp4602Gly
|
|