ENST00000477226.6:n.248G>A
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ENST00000683013.1:n.162G>A
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ENST00000373960.4:c.774G>A
MANE Select
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ENSP00000363071.3:p.Gln258=
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ENST00000373960.3:c.774G>A
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ENSP00000363071.3:p.Gln258=
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ENST00000477226.5:n.246G>A
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|
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ENST00000492726.1:n.169G>A
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NM_001927.3:c.774G>A , LRG_380t1:c.774G>A
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NP_001918.3:p.Gln258=
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NM_001927.4:c.774G>A
MANE Select
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NP_001918.3:p.Gln258=
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NM_001382708.1:c.771G>A
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NP_001369637.1:p.Gln257=
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NM_001382709.1:c.735+187G>A
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NP_001369638.1:n.735+187G>A
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NM_001382710.1:c.774G>A
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NP_001369639.1:p.Gln258=
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NM_001382711.1:c.774G>A
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NP_001369640.1:p.Gln258=
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NM_001382712.1:c.774G>A
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NP_001369641.1:p.Gln258=
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NM_001382713.1:c.504G>A
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NP_001369642.1:p.Gln168=
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