ENST00000217381.3:c.1498_1499delinsCG
MANE Select
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ENSP00000217381.2:p.Arg500=
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ENST00000217381.2:c.1498_1499delinsCG
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ENSP00000217381.2:p.Arg500=
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NM_003098.2:c.1498_1499delinsCG , LRG_332t1:c.1498_1499delinsCG
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NP_003089.1:p.Arg500=
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XM_005260517.1:c.1495_1496delinsCG
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XP_005260574.1:p.Arg499=
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XM_011529007.1:c.*39_*40delinsCG
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XP_011527309.1:n.*39_*40delinsCG
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XM_011529008.1:c.*39_*40delinsCG
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XP_011527310.1:n.*39_*40delinsCG
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XR_936612.1:n.1534_1535delinsCG
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XM_024451971.1:c.1171_1172delinsCG
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XP_024307739.1:p.Arg391=
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NM_003098.3:c.1498_1499delinsCG
MANE Select
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NP_003089.1:p.Arg500=
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