ENST00000476274.7:n.919A>C
|
|
|
ENST00000643029.1:c.*2094A>C
|
ENSP00000496586.1:n.*2094A>C
|
|
ENST00000643338.1:c.*1983A>C
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ENSP00000495890.1:n.*1983A>C
|
|
ENST00000644144.2:c.419A>C
MANE Select
|
ENSP00000494600.1:p.Asp140Ala
|
|
ENST00000645007.1:c.*2343A>C
|
ENSP00000494773.1:n.*2343A>C
|
|
ENST00000646171.1:c.*452A>C
|
ENSP00000495484.1:n.*452A>C
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|
ENST00000223836.10:c.467A>C
|
ENSP00000223836.10:p.Asp156Ala
|
|
ENST00000373156.5:c.419A>C
|
ENSP00000362249.1:p.Asp140Ala
|
|
ENST00000373176.5:c.419A>C
|
ENSP00000362271.1:p.Asp140Ala
|
|
ENST00000413016.5:c.241A>C
|
|
|
ENST00000550143.5:c.199A>C
|
ENSP00000449130.1:n.199A>C
|
|
NM_000476.2:c.419A>C
|
NP_000467.1:p.Asp140Ala
|
|
XM_005251786.2:c.467A>C
|
XP_005251843.1:p.Asp156Ala
|
|
XM_011518348.1:c.419A>C
|
XP_011516650.1:p.Asp140Ala
|
|
XM_011518349.1:c.239A>C
|
XP_011516651.1:p.Asp80Ala
|
|
NM_001318121.1:c.419A>C
|
NP_001305050.1:p.Asp140Ala
|
|
NM_001318122.1:c.467A>C
|
NP_001305051.1:p.Asp156Ala
|
|
XM_017014428.1:c.419A>C
|
XP_016869917.1:p.Asp140Ala
|
|
XM_024447439.1:c.398A>C
|
XP_024303207.1:p.Asp133Ala
|
|
XM_024447440.1:c.239A>C
|
XP_024303208.1:p.Asp80Ala
|
|
NM_001318122.2:c.467A>C
|
NP_001305051.1:p.Asp156Ala
|
|
NM_000476.3:c.419A>C
MANE Select
|
NP_000467.1:p.Asp140Ala
|
|
NR_174625.1:n.3738A>C
|
|
|
NR_174626.1:n.3581A>C
|
|
|
NR_174627.1:n.3618A>C
|
|
|
NR_174628.1:n.2996A>C
|
|
|
NR_174629.1:n.2941A>C
|
|
|
NR_174630.1:n.2977A>C
|
|
|
NR_174631.1:n.2922A>C
|
|
|
NR_174632.1:n.3011A>C
|
|
|