ENST00000255078.8:c.2546C>G
MANE Select
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ENSP00000255078.4:p.Ala849Gly
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ENST00000674675.1:c.691C>G
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ENST00000674878.1:c.651C>G
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ENST00000675118.1:c.2034C>G
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ENST00000675389.1:n.821C>G
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ENST00000675615.1:c.2546C>G
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ENSP00000502413.1:p.Ala849Gly
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ENST00000675648.1:n.1921C>G
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ENST00000675916.1:c.790C>G
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ENST00000676173.1:n.3291C>G
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ENST00000676182.1:c.977C>G
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ENST00000676228.1:c.*1869C>G
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ENSP00000502375.1:n.*1869C>G
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ENST00000255078.7:c.2546C>G
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ENSP00000255078.3:p.Ala849Gly
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ENST00000539064.5:n.2305C>G
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ENST00000543739.5:n.1539C>G
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NM_002180.2:c.2546C>G , LRG_250t1:c.2546C>G
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NP_002171.2:p.Ala849Gly
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XM_005273974.2:c.1535C>G
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XP_005274031.1:p.Ala512Gly
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XM_005273975.2:c.1418C>G
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XP_005274032.1:p.Ala473Gly
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XM_011544994.1:c.1313C>G
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XP_011543296.1:p.Ala438Gly
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XR_949903.1:n.2648C>G
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XM_005273975.3:c.1418C>G
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XP_005274032.1:p.Ala473Gly
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XM_017017669.2:c.1535C>G
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XP_016873158.1:p.Ala512Gly
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XM_017017670.2:c.1535C>G
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XP_016873159.1:p.Ala512Gly
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XR_949903.3:n.2644C>G
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NM_002180.3:c.2546C>G
MANE Select
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NP_002171.2:p.Ala849Gly
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