ENST00000344408.10:c.1853C=
MANE Select
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ENSP00000342144.5:p.Ala618=
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ENST00000310917.6:c.1613C=
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ENSP00000311683.2:p.Ala538=
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ENST00000344408.9:c.1853C=
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ENSP00000342144.5:p.Ala618=
|
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ENST00000475313.5:c.1613C=
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ENSP00000431981.1:p.Ala538=
|
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ENST00000509670.1:c.*246C=
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ENSP00000423876.1:n.*246C=
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NM_001166136.1:c.1613C=
|
NP_001159608.1:p.Ala538=
|
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NM_147127.4:c.1853C=
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NP_667338.3:p.Ala618=
|
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XM_011513392.1:c.1862C=
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XP_011511694.1:p.Ala621=
|
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XM_011513393.1:c.1862C=
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XP_011511695.1:p.Ala621=
|
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XM_011513394.1:c.1622C=
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XP_011511696.1:p.Ala541=
|
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XM_017007736.1:c.1613C=
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XP_016863225.1:p.Ala538=
|
|
XM_017007737.1:c.1613C=
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XP_016863226.1:p.Ala538=
|
|
XM_017007738.1:c.1853C=
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XP_016863227.1:p.Ala618=
|
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XM_017007739.1:c.173C=
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XP_016863228.1:p.Ala58=
|
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XM_024453893.1:c.173C=
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XP_024309661.1:p.Ala58=
|
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XR_001741141.1:n.1918C=
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|
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NM_147127.5:c.1853C=
MANE Select
|
NP_667338.3:p.Ala618=
|
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NM_001166136.2:c.1613C=
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NP_001159608.1:p.Ala538=
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