ENST00000346342.8:c.1151G>C
MANE Select
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ENSP00000329546.4:p.Gly384Ala
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ENST00000346342.7:c.1151G>C
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ENSP00000329546.3:p.Gly384Ala
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ENST00000375581.3:c.1217G>C
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ENSP00000364731.3:p.Gly406Ala
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ENST00000541084.5:c.965G>C
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ENSP00000442051.2:p.Gly322Ala
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NM_000131.4:c.1217G>C , LRG_554t1:c.1217G>C
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NP_000122.1:p.Gly406Ala
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NM_001267554.1:c.965G>C
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NP_001254483.1:p.Gly322Ala
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NM_019616.3:c.1151G>C , LRG_554t2:c.1151G>C
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NP_062562.1:p.Gly384Ala
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NR_051961.1:n.1238G>C
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XM_006719963.2:c.1010G>C
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XP_006720026.1:p.Gly337Ala
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XM_011537474.1:c.1259G>C
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XP_011535776.1:p.Gly420Ala
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XM_011537475.1:c.1073G>C
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XP_011535777.1:p.Gly358Ala
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XM_011537476.1:c.911G>C
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XP_011535778.1:p.Gly304Ala
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XM_011537477.1:c.1220G>C
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XP_011535779.1:p.Gly407Ala
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XM_006719963.3:c.1055G>C
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XP_006720026.2:p.Gly352Ala
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XM_011537474.2:c.1304G>C
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XP_011535776.2:p.Gly435Ala
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XM_011537475.2:c.1118G>C
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XP_011535777.2:p.Gly373Ala
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XM_011537476.2:c.911G>C
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XP_011535778.1:p.Gly304Ala
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NM_019616.4:c.1151G>C
MANE Select
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NP_062562.1:p.Gly384Ala
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NR_051961.2:n.1235G>C
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NM_001267554.2:c.965G>C
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NP_001254483.1:p.Gly322Ala
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