ENST00000697843.1:n.2773G>A
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|
|
ENST00000373189.6:c.1297G>A
MANE Select
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ENSP00000362285.5:p.Ala433Thr
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|
ENST00000479577.2:c.1063G>A
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ENSP00000493995.1:p.Ala355Thr
|
|
ENST00000642198.1:c.*869G>A
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ENSP00000494827.1:n.*869G>A
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ENST00000642772.1:c.*94+6234G>A
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ENSP00000495041.1:n.*94+6234G>A
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|
ENST00000643042.1:c.918G>A
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ENSP00000496674.1:n.918G>A
|
|
ENST00000643619.1:c.*880G>A
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ENSP00000494378.1:n.*880G>A
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|
ENST00000643752.1:c.*623G>A
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ENSP00000495000.1:n.*623G>A
|
|
ENST00000644088.1:c.*618G>A
|
ENSP00000494066.1:n.*618G>A
|
|
ENST00000644591.1:c.*623G>A
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ENSP00000496664.1:n.*623G>A
|
|
ENST00000644895.1:c.*99+6234G>A
|
ENSP00000493872.1:n.*99+6234G>A
|
|
ENST00000645345.1:c.*869G>A
|
ENSP00000495859.1:n.*869G>A
|
|
ENST00000647524.1:c.*880G>A
|
ENSP00000495077.1:n.*880G>A
|
|
ENST00000373189.5:c.1297G>A
|
ENSP00000362285.5:p.Ala433Thr
|
|
ENST00000469204.1:n.794G>A
|
|
|
NM_001174098.1:c.*526G>A
|
NP_001167569.1:n.*526G>A
|
|
NM_018344.5:c.1297G>A
|
NP_060814.4:p.Ala433Thr
|
|
NR_033413.1:n.1271G>A
|
|
|
NR_033414.1:n.1044G>A
|
|
|
XM_006717910.2:c.1063G>A
|
XP_006717973.1:p.Ala355Thr
|
|
NM_001363518.1:c.1063G>A
|
NP_001350447.1:p.Ala355Thr
|
|
XM_017016377.2:c.859G>A
|
XP_016871866.1:p.Ala287Thr
|
|
XM_017016378.2:c.679G>A
|
XP_016871867.1:p.Ala227Thr
|
|
NM_018344.6:c.1297G>A
MANE Select
|
NP_060814.4:p.Ala433Thr
|
|
NM_001174098.2:c.*526G>A
|
NP_001167569.1:n.*526G>A
|
|
NM_001363518.2:c.1063G>A
|
NP_001350447.1:p.Ala355Thr
|
|
NR_033413.2:n.1265G>A
|
|
|
NR_033414.2:n.1038G>A
|
|
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