ENST00000361983.7:c.597A>G
MANE Select
|
ENSP00000354848.4:p.Arg199=
|
|
ENST00000625461.2:n.627A>G
|
|
|
ENST00000626493.2:c.597A>G
|
ENSP00000486692.1:p.Arg199=
|
|
ENST00000635779.2:c.597A>G
|
ENSP00000489663.1:p.Arg199=
|
|
ENST00000635971.2:c.597A>G
|
ENSP00000489878.2:p.Arg199=
|
|
ENST00000636200.2:c.597A>G
|
ENSP00000490113.2:p.Arg199=
|
|
ENST00000637101.2:c.*170A>G
|
ENSP00000490704.1:n.*170A>G
|
|
ENST00000637104.2:c.*166A>G
|
ENSP00000490019.2:n.*166A>G
|
|
ENST00000637323.2:c.*238A>G
|
ENSP00000489659.2:n.*238A>G
|
|
ENST00000637420.2:c.597A>G
|
ENSP00000490404.2:p.Arg199=
|
|
ENST00000637738.2:c.597A>G
|
ENSP00000490742.2:p.Arg199=
|
|
ENST00000638119.2:c.672A>G
|
ENSP00000490026.1:p.Arg224=
|
|
ENST00000674660.1:c.546A>G
|
ENSP00000502562.1:p.Arg182=
|
|
ENST00000674688.1:n.627A>G
|
|
|
ENST00000674897.1:c.81A>G
|
ENSP00000502225.1:p.Arg27=
|
|
ENST00000674936.1:c.597A>G
|
ENSP00000502484.1:p.Arg199=
|
|
ENST00000675576.1:c.498A>G
|
ENSP00000502750.1:p.Arg166=
|
|
ENST00000676080.1:c.*110A>G
|
ENSP00000502706.1:n.*110A>G
|
|
ENST00000361983.6:c.597A>G
|
ENSP00000354848.4:p.Arg199=
|
|
ENST00000625461.1:n.313A>G
|
|
|
ENST00000626493.1:c.597A>G
|
ENSP00000486692.1:p.Arg199=
|
|
NM_015634.3:c.597A>G
|
NP_056449.1:p.Arg199=
|
|
NM_015634.4:c.597A>G
MANE Select
|
NP_056449.1:p.Arg199=
|
|