ENST00000367651.4:c.533G>C
MANE Select
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ENSP00000356623.2:p.Gly178Ala
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ENST00000367651.3:c.533G>C
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ENSP00000356623.2:p.Gly178Ala
|
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ENST00000536159.2:c.533G>C
|
ENSP00000442831.1:p.Gly178Ala
|
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ENST00000537332.2:c.548G>C
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ENSP00000444198.2:p.Gly183Ala
|
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ENST00000618718.1:c.476+57G>C
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ENSP00000479918.1:n.476+57G>C
|
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NM_001168388.2:c.533G>C
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NP_001161860.1:p.Gly178Ala
|
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NM_001168389.2:c.548G>C
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NP_001161861.2:p.Gly183Ala
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NM_006079.4:c.533G>C
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NP_006070.2:p.Gly178Ala
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NM_006079.5:c.533G>C
MANE Select
|
NP_006070.2:p.Gly178Ala
|
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NM_001168388.3:c.533G>C
|
NP_001161860.1:p.Gly178Ala
|
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NM_001168389.3:c.548G>C
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NP_001161861.2:p.Gly183Ala
|
|