ENST00000374580.10:c.1366_1367delinsGA
MANE Select
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ENSP00000363708.4:p.Glu456=
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ENST00000638587.1:c.1297_1298delinsGA
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ENSP00000491062.1:p.Glu433=
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ENST00000374574.2:c.1366_1367delinsGA
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ENSP00000363702.2:p.Glu456=
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ENST00000374580.8:c.1366_1367delinsGA
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ENSP00000363708.4:p.Glu456=
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NM_001204.6:c.1366_1367delinsGA , LRG_712t1:c.1366_1367delinsGA
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NP_001195.2:p.Glu456=
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XM_011511687.1:c.1366_1367delinsGA
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XP_011509989.1:p.Glu456=
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XM_011511688.1:c.1366_1367delinsGA
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XP_011509990.1:p.Glu456=
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NM_001204.7:c.1366_1367delinsGA
MANE Select
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NP_001195.2:p.Glu456=
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