ENST00000295497.13:c.322G>T
|
ENSP00000295497.7:p.Gly108Ter
|
|
ENST00000444394.7:c.322G>T
|
ENSP00000411911.2:p.Gly108Ter
|
|
ENST00000295497.12:c.322G>T
|
ENSP00000295497.7:p.Gly108Ter
|
|
ENST00000409089.7:c.22G>T
|
ENSP00000386322.3:p.Gly8Ter
|
|
ENST00000409900.9:c.697G>T
MANE Select
|
ENSP00000386741.4:p.Gly233Ter
|
|
ENST00000413882.6:c.151G>T
|
ENSP00000410496.2:p.Gly51Ter
|
|
ENST00000425395.6:c.*144G>T
|
ENSP00000405270.2:n.*144G>T
|
|
ENST00000443238.6:c.175G>T
|
ENSP00000409798.2:p.Gly59Ter
|
|
ENST00000444394.6:c.322G>T
|
ENSP00000411911.2:p.Gly108Ter
|
|
ENST00000444573.2:c.541G>T
|
ENSP00000392603.2:p.Gly181Ter
|
|
ENST00000488080.6:n.340G>T
|
|
|
ENST00000650731.1:c.22G>T
|
ENSP00000499146.1:p.Gly8Ter
|
|
ENST00000650938.1:c.221G>T
|
|
|
ENST00000651246.1:c.289G>T
|
ENSP00000498484.1:p.Gly97Ter
|
|
ENST00000651373.1:c.211G>T
|
ENSP00000499174.1:p.Gly71Ter
|
|
ENST00000651501.1:c.*144G>T
|
ENSP00000498894.1:n.*144G>T
|
|
ENST00000651717.1:c.253-11967G>T
|
ENSP00000499124.1:n.253-11967G>T
|
|
ENST00000652036.1:c.322G>T
|
ENSP00000499139.1:p.Gly108Ter
|
|
ENST00000652154.1:n.595G>T
|
|
|
ENST00000295497.11:c.322G>T
|
ENSP00000295497.7:p.Gly108Ter
|
|
ENST00000409089.6:c.22G>T
|
ENSP00000386322.2:p.Gly8Ter
|
|
ENST00000409156.7:c.619G>T
|
ENSP00000386470.3:p.Gly207Ter
|
|
ENST00000409597.5:c.145G>T
|
ENSP00000386469.1:p.Gly49Ter
|
|
ENST00000409900.7:c.697G>T
|
ENSP00000386741.3:p.Gly233Ter
|
|
ENST00000413882.5:c.151G>T
|
ENSP00000410496.1:p.Gly51Ter
|
|
ENST00000425395.5:c.*248G>T
|
ENSP00000405270.1:n.*248G>T
|
|
ENST00000443238.5:c.175G>T
|
ENSP00000409798.1:p.Gly59Ter
|
|
ENST00000444394.5:c.22G>T
|
ENSP00000411911.1:p.Gly8Ter
|
|
ENST00000444573.1:c.322G>T
|
ENSP00000392603.1:p.Gly108Ter
|
|
ENST00000485882.1:n.156G>T
|
|
|
ENST00000488080.5:n.548G>T
|
|
|
NM_001025201.3:c.619G>T
|
NP_001020372.2:p.Gly207Ter
|
|
NM_001206602.1:c.322G>T
|
NP_001193531.1:p.Gly108Ter
|
|
NM_001822.5:c.697G>T
|
NP_001813.1:p.Gly233Ter
|
|
NR_038133.1:n.563G>T
|
|
|
NM_001025201.4:c.619G>T
|
NP_001020372.2:p.Gly207Ter
|
|
NM_001206602.2:c.322G>T
|
NP_001193531.1:p.Gly108Ter
|
|
NM_001371513.1:c.697G>T
|
NP_001358442.1:p.Gly233Ter
|
|
NM_001371514.1:c.748G>T
|
NP_001358443.1:p.Gly250Ter
|
|
NM_001822.7:c.697G>T
MANE Select
|
NP_001813.1:p.Gly233Ter
|
|
NR_038133.2:n.565G>T
|
|
|