ENST00000311907.10:c.819G>C
MANE Select
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ENSP00000308541.5:p.Trp273Cys
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ENST00000311907.9:c.819G>C
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ENSP00000308541.5:p.Trp273Cys
|
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ENST00000442468.1:c.789G>C
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ENSP00000387413.1:p.Trp263Cys
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ENST00000530231.5:c.819G>C
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ENSP00000433907.1:p.Trp273Cys
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NM_000506.3:c.819G>C
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NP_000497.1:p.Trp273Cys
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NM_000506.4:c.819G>C , LRG_551t1:c.819G>C
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NP_000497.1:p.Trp273Cys
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NM_001311257.1:c.771G>C
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NP_001298186.1:p.Trp257Cys
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XR_428840.2:n.863G>C
|
|
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XR_428840.4:n.854G>C
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|
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NM_000506.5:c.819G>C
MANE Select
|
NP_000497.1:p.Trp273Cys
|
|
NM_001311257.2:c.771G>C
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NP_001298186.1:p.Trp257Cys
|
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