ENST00000560563.2:n.1834_1836delinsGCT
(ACTC1)
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ENST00000290378.6:c.934_936delinsGCT
(ACTC1)
MANE Select
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ENSP00000290378.4:p.Ala312=
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ENST00000647798.1:n.1028_1030delinsGCT
(ACTC1)
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ENST00000650163.1:n.1014_1016delinsGCT
(ACTC1)
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ENST00000290378.4:c.934_936delinsGCT
(ACTC1)
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ENSP00000290378.4:p.Ala312=
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ENST00000557860.1:n.624_626delinsGCT
(ACTC1)
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NM_005159.4:c.934_936delinsGCT , LRG_388t1:c.934_936delinsGCT
(ACTC1)
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NP_005150.1:p.Ala312=
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NR_120329.1:n.299+13737_299+13739delinsAGC
(GJD2-DT)
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NM_005159.5:c.934_936delinsGCT
(ACTC1)
MANE Select
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NP_005150.1:p.Ala312=
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