ENST00000236671.7:c.1112T>G
MANE Select
|
ENSP00000236671.2:p.Met371Arg
|
|
ENST00000367196.4:c.1007T>G
|
ENSP00000356164.4:p.Met336Arg
|
|
ENST00000427721.3:c.537T>G
|
|
|
ENST00000429746.2:c.1007T>G
|
ENSP00000402586.2:p.Met336Arg
|
|
ENST00000433655.6:c.*278T>G
|
ENSP00000404902.1:n.*278T>G
|
|
ENST00000438213.6:c.1229T>G
|
ENSP00000415036.2:p.Met410Arg
|
|
ENST00000636397.1:c.1071+173T>G
|
ENSP00000489910.1:n.1071+173T>G
|
|
ENST00000636571.1:c.1091T>G
|
ENSP00000490770.1:p.Met364Arg
|
|
ENST00000636579.1:c.72+173T>G
|
ENSP00000490489.1:n.72+173T>G
|
|
ENST00000636615.1:c.1071+173T>G
|
ENSP00000490014.1:n.1071+173T>G
|
|
ENST00000636843.1:c.1106T>G
|
ENSP00000490897.1:p.Met369Arg
|
|
ENST00000637158.1:n.710T>G
|
|
|
ENST00000637381.2:n.3540T>G
|
|
|
ENST00000637387.1:c.1091T>G
|
ENSP00000490598.1:p.Met364Arg
|
|
ENST00000637815.2:c.1094T>G
|
ENSP00000490344.1:p.Met365Arg
|
|
ENST00000637915.1:c.1103T>G
|
ENSP00000490471.1:p.Met368Arg
|
|
ENST00000637937.1:n.420T>G
|
|
|
ENST00000678991.1:c.*973T>G
|
ENSP00000503019.1:n.*973T>G
|
|
ENST00000236671.6:c.1112T>G
|
ENSP00000236671.2:p.Met371Arg
|
|
ENST00000427721.2:c.471+173T>G
|
ENSP00000415840.2:n.471+173T>G
|
|
ENST00000429746.1:c.443T>G
|
ENSP00000402586.1:p.Met148Arg
|
|
ENST00000433655.5:c.*278T>G
|
ENSP00000404902.1:n.*278T>G
|
|
NM_001909.4:c.1112T>G
|
NP_001900.1:p.Met371Arg
|
|
NM_001909.5:c.1112T>G
MANE Select
|
NP_001900.1:p.Met371Arg
|
|