ENST00000312280.9:c.428T>G
MANE Select
|
ENSP00000308937.3:p.Phe143Cys
|
|
ENST00000395936.7:c.*137T>G
|
ENSP00000379268.1:n.*137T>G
|
|
ENST00000395938.7:c.417T>G
|
ENSP00000379269.3:p.Leu139=
|
|
ENST00000494511.7:c.224T>G
|
ENSP00000462782.2:p.Phe75Cys
|
|
ENST00000580584.3:c.224T>G
|
ENSP00000464468.3:p.Phe75Cys
|
|
ENST00000612492.5:c.428T>G
|
ENSP00000484631.1:p.Phe143Cys
|
|
ENST00000643451.2:c.*283T>G
|
ENSP00000494628.1:n.*283T>G
|
|
ENST00000644020.1:c.*137T>G
|
ENSP00000496522.1:n.*137T>G
|
|
ENST00000646419.2:c.*137T>G
|
ENSP00000494871.1:n.*137T>G
|
|
ENST00000674651.1:c.428T>G
|
ENSP00000501727.1:p.Phe143Cys
|
|
ENST00000674673.1:c.428T>G
|
ENSP00000501804.1:p.Phe143Cys
|
|
ENST00000674707.1:c.224T>G
|
ENSP00000502250.1:p.Phe75Cys
|
|
ENST00000674868.1:c.428T>G
|
ENSP00000502835.1:p.Phe143Cys
|
|
ENST00000674871.1:n.444T>G
|
|
|
ENST00000674947.1:c.417T>G
|
ENSP00000501580.1:p.Leu139=
|
|
ENST00000675197.1:n.408T>G
|
|
|
ENST00000675350.1:c.428T>G
|
ENSP00000501557.1:p.Phe143Cys
|
|
ENST00000675551.1:c.*97T>G
|
ENSP00000501945.1:n.*97T>G
|
|
ENST00000675808.1:c.428T>G
|
ENSP00000502310.1:p.Phe143Cys
|
|
ENST00000675819.1:c.428T>G
|
ENSP00000502018.1:p.Phe143Cys
|
|
ENST00000675854.1:c.224T>G
|
ENSP00000502324.1:p.Phe75Cys
|
|
ENST00000675950.1:c.428T>G
|
ENSP00000501546.1:p.Phe143Cys
|
|
ENST00000676002.1:n.421T>G
|
|
|
ENST00000676161.1:c.287T>G
|
ENSP00000501766.1:p.Phe96Cys
|
|
ENST00000676221.1:c.428T>G
|
ENSP00000502601.1:p.Phe143Cys
|
|
ENST00000676329.1:c.530T>G
|
ENSP00000501698.1:p.Phe177Cys
|
|
ENST00000312280.7:c.428T>G
|
ENSP00000308937.3:p.Phe143Cys
|
|
ENST00000395936.5:c.*137T>G
|
ENSP00000379268.1:n.*137T>G
|
|
ENST00000395938.6:c.428T>G
|
ENSP00000379269.2:p.Phe143Cys
|
|
ENST00000494511.5:c.249T>G
|
ENSP00000462782.1:p.Leu83=
|
|
ENST00000612492.4:c.428T>G
|
ENSP00000484631.1:p.Phe143Cys
|
|
NM_000304.3:c.428T>G
|
NP_000295.1:p.Phe143Cys
|
|
NM_001281455.1:c.428T>G
|
NP_001268384.1:p.Phe143Cys
|
|
NM_001281456.1:c.428T>G
|
NP_001268385.1:p.Phe143Cys
|
|
NM_153321.2:c.428T>G
|
NP_696996.1:p.Phe143Cys
|
|
NM_153322.2:c.428T>G
|
NP_696997.1:p.Phe143Cys
|
|
NR_104017.1:n.554T>G
|
|
|
NR_104018.1:n.454T>G
|
|
|
NM_000304.4:c.428T>G
MANE Select
|
NP_000295.1:p.Phe143Cys
|
|
NM_001281456.2:c.428T>G
|
NP_001268385.1:p.Phe143Cys
|
|
NM_153321.3:c.428T>G
|
NP_696996.1:p.Phe143Cys
|
|
NM_153322.3:c.428T>G
|
NP_696997.1:p.Phe143Cys
|
|
NR_104017.2:n.523T>G
|
|
|
NR_104018.2:n.423T>G
|
|
|
NM_001281455.2:c.428T>G
|
NP_001268384.1:p.Phe143Cys
|
|