ENST00000324041.6:c.544T>A
MANE Select
|
ENSP00000326159.1:p.Tyr182Asn
|
|
ENST00000324041.5:c.544T>A
|
ENSP00000326159.1:p.Tyr182Asn
|
|
ENST00000431178.2:c.328+152T>A
|
ENSP00000399448.2:n.328+152T>A
|
|
ENST00000593885.1:c.*39T>A
|
ENSP00000469769.1:n.*39T>A
|
|
ENST00000596876.1:n.546T>A
|
|
|
ENST00000598305.5:c.*39T>A
|
ENSP00000469963.1:n.*39T>A
|
|
ENST00000599865.5:n.480T>A
|
|
|
ENST00000602148.1:c.556T>A
|
ENSP00000472091.1:n.556T>A
|
|
NM_001302961.1:c.259T>A
|
NP_001289890.1:p.Tyr87Asn
|
|
NM_004917.4:c.544T>A
|
NP_004908.4:p.Tyr182Asn
|
|
NR_126566.1:n.533T>A
|
|
|
XM_005259441.3:c.259T>A
|
XP_005259498.2:p.Tyr87Asn
|
|
XM_011527545.1:c.*39T>A
|
XP_011525847.1:n.*39T>A
|
|
XM_011527546.1:c.475+152T>A
|
XP_011525848.1:n.475+152T>A
|
|
XM_011527547.1:c.397T>A
|
XP_011525849.1:p.Tyr133Asn
|
|
XM_005259441.4:c.259T>A
|
XP_005259498.2:p.Tyr87Asn
|
|
XM_011527545.3:c.*39T>A
|
XP_011525847.1:n.*39T>A
|
|
XM_011527546.2:c.475+152T>A
|
XP_011525848.1:n.475+152T>A
|
|
NM_001302961.2:c.259T>A
|
NP_001289890.1:p.Tyr87Asn
|
|
NR_126566.2:n.533T>A
|
|
|
NM_004917.5:c.544T>A
MANE Select
|
NP_004908.4:p.Tyr182Asn
|
|