ENST00000476274.7:n.918G>T
|
|
|
ENST00000643029.1:c.*2093G>T
|
ENSP00000496586.1:n.*2093G>T
|
|
ENST00000643338.1:c.*1982G>T
|
ENSP00000495890.1:n.*1982G>T
|
|
ENST00000644144.2:c.418G>T
MANE Select
|
ENSP00000494600.1:p.Asp140Tyr
|
|
ENST00000645007.1:c.*2342G>T
|
ENSP00000494773.1:n.*2342G>T
|
|
ENST00000646171.1:c.*451G>T
|
ENSP00000495484.1:n.*451G>T
|
|
ENST00000223836.10:c.466G>T
|
ENSP00000223836.10:p.Asp156Tyr
|
|
ENST00000373156.5:c.418G>T
|
ENSP00000362249.1:p.Asp140Tyr
|
|
ENST00000373176.5:c.418G>T
|
ENSP00000362271.1:p.Asp140Tyr
|
|
ENST00000413016.5:c.240G>T
|
|
|
ENST00000550143.5:c.198G>T
|
ENSP00000449130.1:n.198G>T
|
|
NM_000476.2:c.418G>T
|
NP_000467.1:p.Asp140Tyr
|
|
XM_005251786.2:c.466G>T
|
XP_005251843.1:p.Asp156Tyr
|
|
XM_011518348.1:c.418G>T
|
XP_011516650.1:p.Asp140Tyr
|
|
XM_011518349.1:c.238G>T
|
XP_011516651.1:p.Asp80Tyr
|
|
NM_001318121.1:c.418G>T
|
NP_001305050.1:p.Asp140Tyr
|
|
NM_001318122.1:c.466G>T
|
NP_001305051.1:p.Asp156Tyr
|
|
XM_017014428.1:c.418G>T
|
XP_016869917.1:p.Asp140Tyr
|
|
XM_024447439.1:c.397G>T
|
XP_024303207.1:p.Asp133Tyr
|
|
XM_024447440.1:c.238G>T
|
XP_024303208.1:p.Asp80Tyr
|
|
NM_001318122.2:c.466G>T
|
NP_001305051.1:p.Asp156Tyr
|
|
NM_000476.3:c.418G>T
MANE Select
|
NP_000467.1:p.Asp140Tyr
|
|
NR_174625.1:n.3737G>T
|
|
|
NR_174626.1:n.3580G>T
|
|
|
NR_174627.1:n.3617G>T
|
|
|
NR_174628.1:n.2995G>T
|
|
|
NR_174629.1:n.2940G>T
|
|
|
NR_174630.1:n.2976G>T
|
|
|
NR_174631.1:n.2921G>T
|
|
|
NR_174632.1:n.3010G>T
|
|
|