ENST00000346342.8:c.825C>A
MANE Select
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ENSP00000329546.4:p.Gly275=
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ENST00000346342.7:c.825C>A
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ENSP00000329546.3:p.Gly275=
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ENST00000375581.3:c.891C>A
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ENSP00000364731.3:p.Gly297=
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ENST00000541084.5:c.639C>A
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ENSP00000442051.2:p.Gly213=
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NM_000131.4:c.891C>A , LRG_554t1:c.891C>A
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NP_000122.1:p.Gly297=
|
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NM_001267554.1:c.639C>A
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NP_001254483.1:p.Gly213=
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NM_019616.3:c.825C>A , LRG_554t2:c.825C>A
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NP_062562.1:p.Gly275=
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NR_051961.1:n.912C>A
|
|
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XM_006719963.2:c.684C>A
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XP_006720026.1:p.Gly228=
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XM_011537474.1:c.933C>A
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XP_011535776.1:p.Gly311=
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XM_011537475.1:c.747C>A
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XP_011535777.1:p.Gly249=
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XM_011537476.1:c.585C>A
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XP_011535778.1:p.Gly195=
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XM_011537477.1:c.894C>A
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XP_011535779.1:p.Gly298=
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XM_006719963.3:c.729C>A
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XP_006720026.2:p.Gly243=
|
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XM_011537474.2:c.978C>A
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XP_011535776.2:p.Gly326=
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XM_011537475.2:c.792C>A
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XP_011535777.2:p.Gly264=
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XM_011537476.2:c.585C>A
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XP_011535778.1:p.Gly195=
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NM_019616.4:c.825C>A
MANE Select
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NP_062562.1:p.Gly275=
|
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NR_051961.2:n.909C>A
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|
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NM_001267554.2:c.639C>A
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NP_001254483.1:p.Gly213=
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