ENST00000311907.10:c.775G>C
MANE Select
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ENSP00000308541.5:p.Glu259Gln
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ENST00000311907.9:c.775G>C
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ENSP00000308541.5:p.Glu259Gln
|
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ENST00000442468.1:c.745G>C
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ENSP00000387413.1:p.Glu249Gln
|
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ENST00000530231.5:c.775G>C
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ENSP00000433907.1:p.Glu259Gln
|
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NM_000506.3:c.775G>C
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NP_000497.1:p.Glu259Gln
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NM_000506.4:c.775G>C , LRG_551t1:c.775G>C
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NP_000497.1:p.Glu259Gln
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NM_001311257.1:c.727G>C
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NP_001298186.1:p.Glu243Gln
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XR_428840.2:n.819G>C
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|
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XR_428840.4:n.810G>C
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|
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NM_000506.5:c.775G>C
MANE Select
|
NP_000497.1:p.Glu259Gln
|
|
NM_001311257.2:c.727G>C
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NP_001298186.1:p.Glu243Gln
|
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