ENST00000374580.10:c.1076_1078delinsCTG
MANE Select
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ENSP00000363708.4:p.Thr359=
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ENST00000638587.1:c.1007_1009delinsCTG
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ENSP00000491062.1:p.Thr336=
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ENST00000374574.2:c.1076_1078delinsCTG
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ENSP00000363702.2:p.Thr359=
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ENST00000374580.8:c.1076_1078delinsCTG
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ENSP00000363708.4:p.Thr359=
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NM_001204.6:c.1076_1078delinsCTG , LRG_712t1:c.1076_1078delinsCTG
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NP_001195.2:p.Thr359=
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XM_011511687.1:c.1076_1078delinsCTG
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XP_011509989.1:p.Thr359=
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XM_011511688.1:c.1076_1078delinsCTG
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XP_011509990.1:p.Thr359=
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NM_001204.7:c.1076_1078delinsCTG
MANE Select
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NP_001195.2:p.Thr359=
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