ENST00000311907.10:c.922G>A
MANE Select
|
ENSP00000308541.5:p.Asp308Asn
|
|
ENST00000311907.9:c.922G>A
|
ENSP00000308541.5:p.Asp308Asn
|
|
ENST00000442468.1:c.892G>A
|
ENSP00000387413.1:p.Asp298Asn
|
|
ENST00000530231.5:c.922G>A
|
ENSP00000433907.1:p.Asp308Asn
|
|
NM_000506.3:c.922G>A
|
NP_000497.1:p.Asp308Asn
|
|
NM_000506.4:c.922G>A , LRG_551t1:c.922G>A
|
NP_000497.1:p.Asp308Asn
|
|
NM_001311257.1:c.874G>A
|
NP_001298186.1:p.Asp292Asn
|
|
XR_428840.2:n.966G>A
|
|
|
XR_428840.4:n.957G>A
|
|
|
NM_000506.5:c.922G>A
MANE Select
|
NP_000497.1:p.Asp308Asn
|
|
NM_001311257.2:c.874G>A
|
NP_001298186.1:p.Asp292Asn
|
|