ENST00000346342.8:c.1161C>A
MANE Select
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ENSP00000329546.4:p.Ala387=
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ENST00000346342.7:c.1161C>A
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ENSP00000329546.3:p.Ala387=
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ENST00000375581.3:c.1227C>A
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ENSP00000364731.3:p.Ala409=
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ENST00000541084.5:c.975C>A
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ENSP00000442051.2:p.Ala325=
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NM_000131.4:c.1227C>A , LRG_554t1:c.1227C>A
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NP_000122.1:p.Ala409=
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NM_001267554.1:c.975C>A
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NP_001254483.1:p.Ala325=
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NM_019616.3:c.1161C>A , LRG_554t2:c.1161C>A
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NP_062562.1:p.Ala387=
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NR_051961.1:n.1248C>A
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XM_006719963.2:c.1020C>A
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XP_006720026.1:p.Ala340=
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XM_011537474.1:c.1269C>A
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XP_011535776.1:p.Ala423=
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XM_011537475.1:c.1083C>A
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XP_011535777.1:p.Ala361=
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XM_011537476.1:c.921C>A
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XP_011535778.1:p.Ala307=
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XM_011537477.1:c.1230C>A
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XP_011535779.1:p.Ala410=
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XM_006719963.3:c.1065C>A
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XP_006720026.2:p.Ala355=
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XM_011537474.2:c.1314C>A
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XP_011535776.2:p.Ala438=
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XM_011537475.2:c.1128C>A
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XP_011535777.2:p.Ala376=
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XM_011537476.2:c.921C>A
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XP_011535778.1:p.Ala307=
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NM_019616.4:c.1161C>A
MANE Select
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NP_062562.1:p.Ala387=
|
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NR_051961.2:n.1245C>A
|
|
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NM_001267554.2:c.975C>A
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NP_001254483.1:p.Ala325=
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