ENST00000361983.7:c.568G>T
MANE Select
|
ENSP00000354848.4:p.Glu190Ter
|
|
ENST00000625461.2:n.598G>T
|
|
|
ENST00000626493.2:c.568G>T
|
ENSP00000486692.1:p.Glu190Ter
|
|
ENST00000635779.2:c.568G>T
|
ENSP00000489663.1:p.Glu190Ter
|
|
ENST00000635971.2:c.568G>T
|
ENSP00000489878.2:p.Glu190Ter
|
|
ENST00000636200.2:c.568G>T
|
ENSP00000490113.2:p.Glu190Ter
|
|
ENST00000637101.2:c.*141G>T
|
ENSP00000490704.1:n.*141G>T
|
|
ENST00000637104.2:c.*137G>T
|
ENSP00000490019.2:n.*137G>T
|
|
ENST00000637323.2:c.*209G>T
|
ENSP00000489659.2:n.*209G>T
|
|
ENST00000637420.2:c.568G>T
|
ENSP00000490404.2:p.Glu190Ter
|
|
ENST00000637738.2:c.568G>T
|
ENSP00000490742.2:p.Glu190Ter
|
|
ENST00000638119.2:c.643G>T
|
ENSP00000490026.1:p.Glu215Ter
|
|
ENST00000674660.1:c.526-9G>T
|
ENSP00000502562.1:n.526-9G>T
|
|
ENST00000674688.1:n.598G>T
|
|
|
ENST00000674897.1:c.52G>T
|
ENSP00000502225.1:p.Glu18Ter
|
|
ENST00000674936.1:c.568G>T
|
ENSP00000502484.1:p.Glu190Ter
|
|
ENST00000675576.1:c.469G>T
|
ENSP00000502750.1:p.Glu157Ter
|
|
ENST00000676080.1:c.*81G>T
|
ENSP00000502706.1:n.*81G>T
|
|
ENST00000361983.6:c.568G>T
|
ENSP00000354848.4:p.Glu190Ter
|
|
ENST00000625461.1:n.284G>T
|
|
|
ENST00000626493.1:c.568G>T
|
ENSP00000486692.1:p.Glu190Ter
|
|
NM_015634.3:c.568G>T
|
NP_056449.1:p.Glu190Ter
|
|
NM_015634.4:c.568G>T
MANE Select
|
NP_056449.1:p.Glu190Ter
|
|