ENST00000700029.2:c.1228T>C
|
ENSP00000514759.2:p.Tyr410His
|
|
ENST00000710265.1:c.*164T>C
|
ENSP00000518161.1:n.*164T>C
|
|
ENST00000688158.2:n.1870T>C
|
|
|
ENST00000688922.2:c.*965T>C
|
ENSP00000508742.2:n.*965T>C
|
|
ENST00000700021.1:c.1090T>C
|
ENSP00000514757.1:p.Tyr364His
|
|
ENST00000700022.1:c.*474T>C
|
ENSP00000514758.1:n.*474T>C
|
|
ENST00000700023.1:n.2293T>C
|
|
|
ENST00000700024.1:n.2527T>C
|
|
|
ENST00000706954.1:c.1135T>C
|
ENSP00000516674.1:p.Tyr379His
|
|
ENST00000706955.1:c.*1170T>C
|
ENSP00000516675.1:n.*1170T>C
|
|
ENST00000686459.1:c.*721T>C
|
ENSP00000508909.1:n.*721T>C
|
|
ENST00000688158.1:c.*1246T>C
|
ENSP00000509254.1:n.*1246T>C
|
|
ENST00000688308.1:c.1135T>C
|
ENSP00000508752.1:p.Tyr379His
|
|
ENST00000688922.1:c.1056T>C
|
|
|
ENST00000693560.1:c.1654T>C
|
ENSP00000509861.1:p.Tyr552His
|
|
ENST00000371953.8:c.1135T>C
MANE Select
|
ENSP00000361021.3:p.Tyr379His
|
|
ENST00000371953.7:c.1135T>C
|
ENSP00000361021.3:p.Tyr379His
|
|
NM_000314.5:c.1135T>C
|
NP_000305.3:p.Tyr379His
|
|
NM_000314.6:c.1135T>C
|
NP_000305.3:p.Tyr379His
|
|
NM_001304717.2:c.1654T>C
|
NP_001291646.2:p.Tyr552His
|
|
NM_001304718.1:c.544T>C
|
NP_001291647.1:p.Tyr182His
|
|
XM_006717926.2:c.1090T>C
|
XP_006717989.1:p.Tyr364His
|
|
XM_011539982.1:c.1039T>C
|
XP_011538284.1:p.Tyr347His
|
|
XR_945791.1:n.1705T>C
|
|
|
NM_000314.7:c.1135T>C
|
NP_000305.3:p.Tyr379His
|
|
NM_001304717.5:c.1654T>C
|
NP_001291646.4:p.Tyr552His
|
|
NM_001304718.2:c.544T>C
|
NP_001291647.1:p.Tyr182His
|
|
NM_000314.8:c.1135T>C
MANE Select
|
NP_000305.3:p.Tyr379His
|
|