ENST00000593677.2:c.1889A>G
|
|
|
ENST00000688602.1:c.3286A>G
|
|
|
ENST00000689936.1:c.3258A>G
|
|
|
ENST00000692547.1:n.346A>G
|
|
|
ENST00000359596.8:c.14953A>G
MANE Select
|
ENSP00000352608.2:p.Asn4985Asp
|
|
ENST00000355481.8:c.14938A>G
|
ENSP00000347667.3:p.Asn4980Asp
|
|
ENST00000359596.7:c.14953A>G
|
ENSP00000352608.2:p.Asn4985Asp
|
|
ENST00000360985.7:c.14935A>G
|
ENSP00000354254.4:p.Asn4979Asp
|
|
NM_000540.2:c.14953A>G , LRG_766t1:c.14953A>G
|
NP_000531.2:p.Asn4985Asp
|
|
NM_001042723.1:c.14938A>G
|
NP_001036188.1:p.Asn4980Asp
|
|
XM_006723317.1:c.14935A>G
|
XP_006723380.1:p.Asn4979Asp
|
|
XM_006723319.1:c.14920A>G
|
XP_006723382.1:p.Asn4974Asp
|
|
XM_011527204.1:c.14950A>G
|
XP_011525506.1:p.Asn4984Asp
|
|
XM_011527205.1:c.14866A>G
|
XP_011525507.1:p.Asn4956Asp
|
|
XM_006723317.2:c.14935A>G
|
XP_006723380.1:p.Asn4979Asp
|
|
XM_006723319.2:c.14920A>G
|
XP_006723382.1:p.Asn4974Asp
|
|
XM_011527205.2:c.14866A>G
|
XP_011525507.1:p.Asn4956Asp
|
|
NM_000540.3:c.14953A>G
MANE Select
|
NP_000531.2:p.Asn4985Asp
|
|
NM_001042723.2:c.14938A>G
|
NP_001036188.1:p.Asn4980Asp
|
|