ENST00000346342.8:c.306G>T
MANE Select
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ENSP00000329546.4:p.Gln102His
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ENST00000346342.7:c.306G>T
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ENSP00000329546.3:p.Gln102His
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ENST00000375581.3:c.372G>T
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ENSP00000364731.3:p.Gln124His
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ENST00000444337.1:c.*114G>T
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ENSP00000387669.1:n.*114G>T
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ENST00000473085.1:n.253G>T
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ENST00000479674.1:n.639G>T
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ENST00000541084.5:c.120G>T
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ENSP00000442051.2:p.Gln40His
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NM_000131.4:c.372G>T , LRG_554t1:c.372G>T
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NP_000122.1:p.Gln124His
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NM_001267554.1:c.120G>T
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NP_001254483.1:p.Gln40His
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NM_019616.3:c.306G>T , LRG_554t2:c.306G>T
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NP_062562.1:p.Gln102His
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NR_051961.1:n.393G>T
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XM_006719963.2:c.306G>T
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XP_006720026.1:p.Gln102His
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XM_011537474.1:c.306G>T
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XP_011535776.1:p.Gln102His
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XM_011537475.1:c.120G>T
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XP_011535777.1:p.Gln40His
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XM_011537477.1:c.267G>T
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XP_011535779.1:p.Gln89His
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XM_006719963.3:c.351G>T
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XP_006720026.2:p.Gln117His
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XM_011537474.2:c.351G>T
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XP_011535776.2:p.Gln117His
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XM_011537475.2:c.165G>T
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XP_011535777.2:p.Gln55His
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NM_019616.4:c.306G>T
MANE Select
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NP_062562.1:p.Gln102His
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NR_051961.2:n.390G>T
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NM_001267554.2:c.120G>T
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NP_001254483.1:p.Gln40His
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