ENST00000472480.2:n.1497A>C
|
|
|
ENST00000685279.1:c.384A>C
|
ENSP00000509424.1:p.Ala128=
|
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ENST00000688043.1:n.1838A>C
|
|
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ENST00000689668.1:n.1624A>C
|
|
|
ENST00000690876.1:c.1506A>C
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ENSP00000508955.1:p.Ala502=
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ENST00000691229.1:c.1506A>C
|
ENSP00000510437.1:p.Ala502=
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|
ENST00000692089.1:c.1506A>C
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ENSP00000508626.1:p.Ala502=
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|
ENST00000692620.1:c.384A>C
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ENSP00000509311.1:p.Ala128=
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|
ENST00000402219.8:c.1617A>C
MANE Select
|
ENSP00000384675.2:p.Ala539=
|
|
ENST00000395038.6:c.1617A>C
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ENSP00000378479.2:p.Ala539=
|
|
ENST00000402219.6:c.1617A>C
|
ENSP00000384675.2:p.Ala539=
|
|
ENST00000426016.5:c.1617A>C
|
ENSP00000387784.1:p.Ala539=
|
|
NM_005633.3:c.1617A>C , LRG_754t1:c.1617A>C
|
NP_005624.2:p.Ala539=
|
|
XM_005264515.3:c.1617A>C
|
XP_005264572.1:p.Ala539=
|
|
XM_011533060.1:c.1710A>C
|
XP_011531362.1:p.Ala570=
|
|
XM_011533061.1:c.1710A>C
|
XP_011531363.1:p.Ala570=
|
|
XM_011533062.1:c.1596A>C
|
XP_011531364.1:p.Ala532=
|
|
XM_011533063.1:c.1593A>C
|
XP_011531365.1:p.Ala531=
|
|
XM_011533064.1:c.1446A>C
|
XP_011531366.1:p.Ala482=
|
|
XM_011533065.1:c.1710A>C
|
XP_011531367.1:p.Ala570=
|
|
XM_011533066.1:c.552A>C
|
XP_011531368.1:p.Ala184=
|
|
XM_005264515.4:c.1617A>C
|
XP_005264572.1:p.Ala539=
|
|
XM_011533062.2:c.1596A>C
|
XP_011531364.1:p.Ala532=
|
|
XM_011533064.2:c.1446A>C
|
XP_011531366.1:p.Ala482=
|
|
NM_001382394.1:c.1596A>C
|
NP_001369323.1:p.Ala532=
|
|
NM_001382395.1:c.1617A>C
|
NP_001369324.1:p.Ala539=
|
|
NM_005633.4:c.1617A>C
MANE Select
|
NP_005624.2:p.Ala539=
|
|