ENST00000262367.10:c.5422T>G
MANE Select
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ENSP00000262367.5:p.Cys1808Gly
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ENST00000262367.9:c.5422T>G
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ENSP00000262367.5:p.Cys1808Gly
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ENST00000382070.7:c.5308T>G
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ENSP00000371502.3:p.Cys1770Gly
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NM_001079846.1:c.5308T>G
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NP_001073315.1:p.Cys1770Gly
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NM_004380.2:c.5422T>G
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NP_004371.2:p.Cys1808Gly
|
|
XM_005255124.3:c.5377T>G
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XP_005255181.1:p.Cys1793Gly
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XM_005255125.3:c.5005T>G
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XP_005255182.1:p.Cys1669Gly
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XM_006720848.2:c.5161T>G
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XP_006720911.1:p.Cys1721Gly
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XM_011522380.1:c.5368T>G
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XP_011520682.1:p.Cys1790Gly
|
|
XM_011522381.1:c.4669T>G
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XP_011520683.1:p.Cys1557Gly
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XM_005255124.4:c.5377T>G
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XP_005255181.1:p.Cys1793Gly
|
|
XM_005255125.4:c.5005T>G
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XP_005255182.1:p.Cys1669Gly
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XM_006720848.3:c.5161T>G
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XP_006720911.1:p.Cys1721Gly
|
|
XM_011522381.2:c.4669T>G
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XP_011520683.1:p.Cys1557Gly
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XM_017022944.1:c.5416T>G
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XP_016878433.1:p.Cys1806Gly
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NM_004380.3:c.5422T>G
MANE Select
|
NP_004371.2:p.Cys1808Gly
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