ENST00000311907.10:c.846C>A
MANE Select
|
ENSP00000308541.5:p.Asp282Glu
|
|
ENST00000311907.9:c.846C>A
|
ENSP00000308541.5:p.Asp282Glu
|
|
ENST00000442468.1:c.816C>A
|
ENSP00000387413.1:p.Asp272Glu
|
|
ENST00000530231.5:c.846C>A
|
ENSP00000433907.1:p.Asp282Glu
|
|
NM_000506.3:c.846C>A
|
NP_000497.1:p.Asp282Glu
|
|
NM_000506.4:c.846C>A , LRG_551t1:c.846C>A
|
NP_000497.1:p.Asp282Glu
|
|
NM_001311257.1:c.798C>A
|
NP_001298186.1:p.Asp266Glu
|
|
XR_428840.2:n.890C>A
|
|
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XR_428840.4:n.881C>A
|
|
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NM_000506.5:c.846C>A
MANE Select
|
NP_000497.1:p.Asp282Glu
|
|
NM_001311257.2:c.798C>A
|
NP_001298186.1:p.Asp266Glu
|
|