ENST00000262367.10:c.5562G=
MANE Select
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ENSP00000262367.5:p.Gln1854=
|
|
ENST00000262367.9:c.5562G=
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ENSP00000262367.5:p.Gln1854=
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|
ENST00000382070.7:c.5448G=
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ENSP00000371502.3:p.Gln1816=
|
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NM_001079846.1:c.5448G=
|
NP_001073315.1:p.Gln1816=
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|
NM_004380.2:c.5562G=
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NP_004371.2:p.Gln1854=
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|
XM_005255124.3:c.5517G=
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XP_005255181.1:p.Gln1839=
|
|
XM_005255125.3:c.5145G=
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XP_005255182.1:p.Gln1715=
|
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XM_006720848.2:c.5301G=
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XP_006720911.1:p.Gln1767=
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XM_011522380.1:c.5508G=
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XP_011520682.1:p.Gln1836=
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|
XM_011522381.1:c.4809G=
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XP_011520683.1:p.Gln1603=
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|
XM_005255124.4:c.5517G=
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XP_005255181.1:p.Gln1839=
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|
XM_005255125.4:c.5145G=
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XP_005255182.1:p.Gln1715=
|
|
XM_006720848.3:c.5301G=
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XP_006720911.1:p.Gln1767=
|
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XM_011522381.2:c.4809G=
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XP_011520683.1:p.Gln1603=
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|
XM_017022944.1:c.5556G=
|
XP_016878433.1:p.Gln1852=
|
|
NM_004380.3:c.5562G=
MANE Select
|
NP_004371.2:p.Gln1854=
|
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