ENST00000346342.8:c.1089G>C
MANE Select
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ENSP00000329546.4:p.Glu363Asp
|
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ENST00000346342.7:c.1089G>C
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ENSP00000329546.3:p.Glu363Asp
|
|
ENST00000375581.3:c.1155G>C
|
ENSP00000364731.3:p.Glu385Asp
|
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ENST00000541084.5:c.903G>C
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ENSP00000442051.2:p.Glu301Asp
|
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NM_000131.4:c.1155G>C , LRG_554t1:c.1155G>C
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NP_000122.1:p.Glu385Asp
|
|
NM_001267554.1:c.903G>C
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NP_001254483.1:p.Glu301Asp
|
|
NM_019616.3:c.1089G>C , LRG_554t2:c.1089G>C
|
NP_062562.1:p.Glu363Asp
|
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NR_051961.1:n.1176G>C
|
|
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XM_006719963.2:c.948G>C
|
XP_006720026.1:p.Glu316Asp
|
|
XM_011537474.1:c.1197G>C
|
XP_011535776.1:p.Glu399Asp
|
|
XM_011537475.1:c.1011G>C
|
XP_011535777.1:p.Glu337Asp
|
|
XM_011537476.1:c.849G>C
|
XP_011535778.1:p.Glu283Asp
|
|
XM_011537477.1:c.1158G>C
|
XP_011535779.1:p.Glu386Asp
|
|
XM_006719963.3:c.993G>C
|
XP_006720026.2:p.Glu331Asp
|
|
XM_011537474.2:c.1242G>C
|
XP_011535776.2:p.Glu414Asp
|
|
XM_011537475.2:c.1056G>C
|
XP_011535777.2:p.Glu352Asp
|
|
XM_011537476.2:c.849G>C
|
XP_011535778.1:p.Glu283Asp
|
|
NM_019616.4:c.1089G>C
MANE Select
|
NP_062562.1:p.Glu363Asp
|
|
NR_051961.2:n.1173G>C
|
|
|
NM_001267554.2:c.903G>C
|
NP_001254483.1:p.Glu301Asp
|
|