ENST00000236671.7:c.1192G>C
MANE Select
|
ENSP00000236671.2:p.Asp398His
|
|
ENST00000367196.4:c.1087G>C
|
ENSP00000356164.4:p.Asp363His
|
|
ENST00000427721.3:c.617G>C
|
|
|
ENST00000429746.2:c.1087G>C
|
ENSP00000402586.2:p.Asp363His
|
|
ENST00000433655.6:c.*358G>C
|
ENSP00000404902.1:n.*358G>C
|
|
ENST00000438213.6:c.1309G>C
|
ENSP00000415036.2:p.Asp437His
|
|
ENST00000636397.1:c.1071+253G>C
|
ENSP00000489910.1:n.1071+253G>C
|
|
ENST00000636571.1:c.1171G>C
|
ENSP00000490770.1:p.Asp391His
|
|
ENST00000636579.1:c.72+253G>C
|
ENSP00000490489.1:n.72+253G>C
|
|
ENST00000636615.1:c.1071+253G>C
|
ENSP00000490014.1:n.1071+253G>C
|
|
ENST00000636843.1:c.1186G>C
|
ENSP00000490897.1:p.Asp396His
|
|
ENST00000637158.1:n.790G>C
|
|
|
ENST00000637381.2:n.3620G>C
|
|
|
ENST00000637387.1:c.1171G>C
|
ENSP00000490598.1:p.Asp391His
|
|
ENST00000637815.2:c.1174G>C
|
ENSP00000490344.1:p.Asp392His
|
|
ENST00000637915.1:c.1183G>C
|
ENSP00000490471.1:p.Asp395His
|
|
ENST00000637937.1:n.500G>C
|
|
|
ENST00000678991.1:c.*1053G>C
|
ENSP00000503019.1:n.*1053G>C
|
|
ENST00000236671.6:c.1192G>C
|
ENSP00000236671.2:p.Asp398His
|
|
ENST00000427721.2:c.471+253G>C
|
ENSP00000415840.2:n.471+253G>C
|
|
ENST00000429746.1:c.523G>C
|
ENSP00000402586.1:p.Asp175His
|
|
ENST00000433655.5:c.*358G>C
|
ENSP00000404902.1:n.*358G>C
|
|
NM_001909.4:c.1192G>C
|
NP_001900.1:p.Asp398His
|
|
NM_001909.5:c.1192G>C
MANE Select
|
NP_001900.1:p.Asp398His
|
|