ENST00000237596.7:c.984_985delinsTG
MANE Select
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ENSP00000237596.2:p.Asn328=
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ENST00000237596.6:c.984_985delinsTG
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ENSP00000237596.2:p.Asn328=
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ENST00000506367.1:n.431_432delinsTG
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NM_000297.3:c.984_985delinsTG
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NP_000288.1:p.Asn328=
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XM_011532028.1:c.984_985delinsTG
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XP_011530330.1:p.Asn328=
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XM_011532029.1:c.264_265delinsTG
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XP_011530331.1:p.Asn88=
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XM_011532030.1:c.144_145delinsTG
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XP_011530332.1:p.Asn48=
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XR_244632.2:n.1079_1080delinsTG
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NR_156488.1:n.1071_1072delinsTG
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XM_011532028.2:c.984_985delinsTG
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XP_011530330.1:p.Asn328=
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XM_011532030.2:c.144_145delinsTG
|
XP_011530332.1:p.Asn48=
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|
NM_000297.4:c.984_985delinsTG
MANE Select
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NP_000288.1:p.Asn328=
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NR_156488.2:n.1083_1084delinsTG
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