ENST00000311907.10:c.688C>G
MANE Select
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ENSP00000308541.5:p.His230Asp
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ENST00000311907.9:c.688C>G
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ENSP00000308541.5:p.His230Asp
|
|
ENST00000442468.1:c.658C>G
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ENSP00000387413.1:p.His220Asp
|
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ENST00000490274.1:n.468C>G
|
|
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ENST00000530231.5:c.688C>G
|
ENSP00000433907.1:p.His230Asp
|
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NM_000506.3:c.688C>G
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NP_000497.1:p.His230Asp
|
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NM_000506.4:c.688C>G , LRG_551t1:c.688C>G
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NP_000497.1:p.His230Asp
|
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NM_001311257.1:c.640C>G
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NP_001298186.1:p.His214Asp
|
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XR_428840.2:n.732C>G
|
|
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XR_428840.4:n.723C>G
|
|
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NM_000506.5:c.688C>G
MANE Select
|
NP_000497.1:p.His230Asp
|
|
NM_001311257.2:c.640C>G
|
NP_001298186.1:p.His214Asp
|
|