|
NM_001182.5:c.1061A>G
MANE Select
|
NP_001173.2:p.Tyr354Cys
|
|
ENST00000409134.8:c.1061A>G
MANE Select
|
ENSP00000387123.3:p.Tyr354Cys
|
|
NM_001182.4:c.1061A>G
|
NP_001173.2:p.Tyr354Cys
|
|
NM_001201377.1:c.977A>G
|
NP_001188306.1:p.Tyr326Cys
|
|
NM_001201377.2:c.977A>G
|
NP_001188306.1:p.Tyr326Cys
|
|
NM_001202404.1:c.1089+3277A>G
|
NP_001189333.1:n.1089+3277A>G
|
|
NM_001202404.2:c.1008+3277A>G
|
NP_001189333.2:n.1008+3277A>G
|
|
ENST00000409134.7:c.1061A>G
|
ENSP00000387123.3:p.Tyr354Cys
|
|
ENST00000447989.6:c.1089+3277A>G
|
ENSP00000414132.2:n.1089+3277A>G
|
|
ENST00000458249.6:c.*970A>G
|
ENSP00000403929.1:n.*970A>G
|
|
ENST00000497231.6:n.1271A>G
|
|
|
ENST00000497231.7:n.1488A>G
|
|
|
ENST00000503281.5:c.650A>G
|
|
|
ENST00000503281.6:c.650A>G
|
|
|
ENST00000553117.5:c.1008+3277A>G
|
ENSP00000448593.1:n.1008+3277A>G
|
|
ENST00000635851.1:c.1059A>G
|
|
|
ENST00000636062.1:n.956A>G
|
|
|
ENST00000636225.1:c.*1005A>G
|
ENSP00000490797.1:n.*1005A>G
|
|
ENST00000636286.1:n.779A>G
|
|
|
ENST00000636482.1:n.548A>G
|
|
|
ENST00000636743.1:c.941A>G
|
ENSP00000489725.1:p.Tyr314Cys
|
|
ENST00000636808.1:c.*870A>G
|
ENSP00000490833.1:n.*870A>G
|
|
ENST00000636872.1:c.1221A>G
|
ENSP00000490919.1:n.1221A>G
|
|
ENST00000636879.1:c.1106A>G
|
ENSP00000490811.1:p.Tyr369Cys
|
|
ENST00000636886.1:c.860A>G
|
ENSP00000490371.1:p.Tyr287Cys
|
|
ENST00000637206.1:c.914-1570A>G
|
ENSP00000489895.1:n.914-1570A>G
|
|
ENST00000637272.1:c.1052A>G
|
ENSP00000489686.1:p.Tyr351Cys
|
|
ENST00000637292.1:c.634A>G
|
|
|
ENST00000637782.1:c.1061A>G
|
ENSP00000490024.1:p.Tyr354Cys
|
|
ENST00000637964.1:c.1007A>G
|
ENSP00000490291.1:p.Tyr336Cys
|
|
ENST00000638008.1:c.*905A>G
|
ENSP00000490400.1:n.*905A>G
|
|
XM_011543417.1:c.656A>G
|
XP_011541719.1:p.Tyr219Cys
|
|
XM_011543417.2:c.656A>G
|
XP_011541719.1:p.Tyr219Cys
|
