ENST00000346342.8:c.765C>G
MANE Select
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ENSP00000329546.4:p.Asp255Glu
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ENST00000346342.7:c.765C>G
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ENSP00000329546.3:p.Asp255Glu
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ENST00000375581.3:c.831C>G
|
ENSP00000364731.3:p.Asp277Glu
|
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ENST00000541084.5:c.579C>G
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ENSP00000442051.2:p.Asp193Glu
|
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NM_000131.4:c.831C>G , LRG_554t1:c.831C>G
|
NP_000122.1:p.Asp277Glu
|
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NM_001267554.1:c.579C>G
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NP_001254483.1:p.Asp193Glu
|
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NM_019616.3:c.765C>G , LRG_554t2:c.765C>G
|
NP_062562.1:p.Asp255Glu
|
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NR_051961.1:n.852C>G
|
|
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XM_006719963.2:c.624C>G
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XP_006720026.1:p.Asp208Glu
|
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XM_011537474.1:c.873C>G
|
XP_011535776.1:p.Asp291Glu
|
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XM_011537475.1:c.687C>G
|
XP_011535777.1:p.Asp229Glu
|
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XM_011537476.1:c.525C>G
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XP_011535778.1:p.Asp175Glu
|
|
XM_011537477.1:c.834C>G
|
XP_011535779.1:p.Asp278Glu
|
|
XM_006719963.3:c.669C>G
|
XP_006720026.2:p.Asp223Glu
|
|
XM_011537474.2:c.918C>G
|
XP_011535776.2:p.Asp306Glu
|
|
XM_011537475.2:c.732C>G
|
XP_011535777.2:p.Asp244Glu
|
|
XM_011537476.2:c.525C>G
|
XP_011535778.1:p.Asp175Glu
|
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NM_019616.4:c.765C>G
MANE Select
|
NP_062562.1:p.Asp255Glu
|
|
NR_051961.2:n.849C>G
|
|
|
NM_001267554.2:c.579C>G
|
NP_001254483.1:p.Asp193Glu
|
|