ENST00000585362.7:c.665A>C
|
ENSP00000473614.3:p.Glu222Ala
|
|
ENST00000593032.6:c.534A>C
|
ENSP00000465828.4:p.Gly178=
|
|
ENST00000706713.1:c.548A>C
|
ENSP00000516510.1:p.Glu183Ala
|
|
ENST00000706714.1:c.534A>C
|
ENSP00000516511.1:p.Gly178=
|
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ENST00000706715.1:c.170A>C
|
ENSP00000516512.1:p.Glu57Ala
|
|
ENST00000354171.13:c.554A>C
MANE Select
|
ENSP00000346103.7:p.Glu185Ala
|
|
ENST00000589115.6:c.529A>C
|
ENSP00000466872.3:p.Ser177Arg
|
|
ENST00000354171.12:c.554A>C
|
ENSP00000346103.7:p.Glu185Ala
|
|
ENST00000585480.1:c.287A>C
|
ENSP00000467900.1:p.Glu96Ala
|
|
ENST00000587648.5:c.434A>C
|
ENSP00000468349.1:p.Glu145Ala
|
|
ENST00000588919.5:c.495A>C
|
ENSP00000464989.3:p.Gly165=
|
|
ENST00000589115.5:c.529A>C
|
ENSP00000466872.2:p.Ser177Arg
|
|
ENST00000592940.2:n.925A>C
|
|
|
ENST00000611653.4:c.473A>C
|
ENSP00000483655.1:p.Glu158Ala
|
|
ENST00000616066.4:c.551A>C
|
ENSP00000485000.1:p.Glu184Ala
|
|
ENST00000622390.4:c.662A>C
|
ENSP00000477503.1:p.Glu221Ala
|
|
NM_001039847.2:c.576A>C
|
NP_001034936.1:p.Gly192=
|
|
NM_001039848.2:c.665A>C
|
NP_001034937.1:p.Glu222Ala
|
|
NM_002085.4:c.554A>C
|
NP_002076.2:p.Glu185Ala
|
|
NM_001039848.3:c.665A>C
|
NP_001034937.1:p.Glu222Ala
|
|
NM_001039847.3:c.576A>C
|
NP_001034936.1:p.Gly192=
|
|
NM_001039848.4:c.665A>C
|
NP_001034937.1:p.Glu222Ala
|
|
NM_001367832.1:c.473A>C
|
NP_001354761.1:p.Glu158Ala
|
|
NM_002085.5:c.554A>C
MANE Select
|
NP_002076.2:p.Glu185Ala
|
|