ENST00000262367.10:c.5527T>G
MANE Select
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ENSP00000262367.5:p.Cys1843Gly
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ENST00000262367.9:c.5527T>G
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ENSP00000262367.5:p.Cys1843Gly
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ENST00000382070.7:c.5413T>G
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ENSP00000371502.3:p.Cys1805Gly
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NM_001079846.1:c.5413T>G
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NP_001073315.1:p.Cys1805Gly
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NM_004380.2:c.5527T>G
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NP_004371.2:p.Cys1843Gly
|
|
XM_005255124.3:c.5482T>G
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XP_005255181.1:p.Cys1828Gly
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XM_005255125.3:c.5110T>G
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XP_005255182.1:p.Cys1704Gly
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XM_006720848.2:c.5266T>G
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XP_006720911.1:p.Cys1756Gly
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XM_011522380.1:c.5473T>G
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XP_011520682.1:p.Cys1825Gly
|
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XM_011522381.1:c.4774T>G
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XP_011520683.1:p.Cys1592Gly
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XM_005255124.4:c.5482T>G
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XP_005255181.1:p.Cys1828Gly
|
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XM_005255125.4:c.5110T>G
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XP_005255182.1:p.Cys1704Gly
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XM_006720848.3:c.5266T>G
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XP_006720911.1:p.Cys1756Gly
|
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XM_011522381.2:c.4774T>G
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XP_011520683.1:p.Cys1592Gly
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XM_017022944.1:c.5521T>G
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XP_016878433.1:p.Cys1841Gly
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NM_004380.3:c.5527T>G
MANE Select
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NP_004371.2:p.Cys1843Gly
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