ENST00000254108.12:c.878G>C
MANE Select
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ENSP00000254108.8:p.Gly293Ala
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ENST00000254108.11:c.878G>C
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ENSP00000254108.7:p.Gly293Ala
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ENST00000380244.7:c.875G>C
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ENSP00000369594.3:p.Gly292Ala
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ENST00000474990.5:n.172G>C
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ENST00000487509.6:n.4053G>C
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ENST00000564766.1:n.702G>C
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ENST00000566605.5:c.*51G>C
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ENSP00000455073.1:n.*51G>C
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ENST00000568685.1:c.881G>C
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ENSP00000455282.1:p.Gly294Ala
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ENST00000568901.2:n.252G>C
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NM_001170634.1:c.875G>C
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NP_001164105.1:p.Gly292Ala
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NM_001170937.1:c.866G>C
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NP_001164408.1:p.Gly289Ala
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NM_004960.3:c.878G>C , LRG_655t1:c.878G>C
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NP_004951.1:p.Gly293Ala
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NR_028388.2:n.948G>C
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XM_005255233.3:c.263G>C
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XP_005255290.1:p.Gly88Ala
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XM_011545781.1:c.872G>C
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XP_011544083.1:p.Gly291Ala
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XM_011545782.1:c.263G>C
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XP_011544084.1:p.Gly88Ala
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XM_005255233.5:c.263G>C
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XP_005255290.1:p.Gly88Ala
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XM_011545782.2:c.263G>C
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XP_011544084.1:p.Gly88Ala
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XM_024450221.1:c.869G>C
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XP_024305989.1:p.Gly290Ala
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NM_004960.4:c.878G>C
MANE Select
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NP_004951.1:p.Gly293Ala
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