ENST00000421834.7:c.7942G>A
|
ENSP00000400883.3:p.Ala2648Thr
|
|
ENST00000449297.7:c.8476G>A
|
ENSP00000393082.3:p.Ala2826Thr
|
|
ENST00000520645.6:c.8062G>A
|
ENSP00000431030.2:p.Ala2688Thr
|
|
ENST00000520144.2:n.804G>A
|
|
|
ENST00000680361.1:c.14833G>A
MANE Select
|
ENSP00000505098.1:p.Ala4945Thr
|
|
ENST00000244364.10:c.6964G>A
|
ENSP00000244364.6:p.Ala2322Thr
|
|
ENST00000312431.10:c.8062G>A
|
ENSP00000307959.7:p.Ala2688Thr
|
|
ENST00000361203.7:c.14200G>A
|
ENSP00000354508.3:p.Ala4734Thr
|
|
ENST00000370754.9:c.8476G>A
|
ENSP00000359790.6:p.Ala2826Thr
|
|
ENST00000370788.6:c.7942G>A
|
ENSP00000359824.2:p.Ala2648Thr
|
|
ENST00000421834.6:c.7942G>A
|
ENSP00000400883.3:p.Ala2648Thr
|
|
ENST00000520144.1:n.542G>A
|
|
|
NM_001144769.2:c.8476G>A
|
NP_001138241.1:p.Ala2826Thr
|
|
NM_001144770.1:c.8062G>A
|
NP_001138242.1:p.Ala2688Thr
|
|
NM_015548.4:c.6964G>A
|
NP_056363.2:p.Ala2322Thr
|
|
NM_183380.3:c.7942G>A
|
NP_899236.1:p.Ala2648Thr
|
|
XM_005249310.2:c.14833G>A
|
XP_005249367.1:p.Ala4945Thr
|
|
XM_005249315.2:c.14734G>A
|
XP_005249372.1:p.Ala4912Thr
|
|
XM_005249316.1:c.14548G>A
|
XP_005249373.1:p.Ala4850Thr
|
|
XM_005249318.1:c.14419G>A
|
XP_005249375.1:p.Ala4807Thr
|
|
XM_005249319.1:c.14320G>A
|
XP_005249376.1:p.Ala4774Thr
|
|
XM_005249320.3:c.14299G>A
|
XP_005249377.1:p.Ala4767Thr
|
|
XM_005249322.3:c.14278G>A
|
XP_005249379.1:p.Ala4760Thr
|
|
XM_005249323.2:c.14200G>A
|
XP_005249380.1:p.Ala4734Thr
|
|
XM_005249324.1:c.13222G>A
|
XP_005249381.1:p.Ala4408Thr
|
|
XM_011514824.1:c.14761G>A
|
XP_011513126.1:p.Ala4921Thr
|
|
XM_011514825.1:c.8503G>A
|
XP_011513127.1:p.Ala2835Thr
|
|
XM_011514826.1:c.14200G>A
|
XP_011513128.1:p.Ala4734Thr
|
|
XM_005249310.4:c.14833G>A
|
XP_005249367.1:p.Ala4945Thr
|
|
XM_005249315.3:c.14734G>A
|
XP_005249372.1:p.Ala4912Thr
|
|
XM_005249316.3:c.14548G>A
|
XP_005249373.1:p.Ala4850Thr
|
|
XM_005249318.2:c.14419G>A
|
XP_005249375.1:p.Ala4807Thr
|
|
XM_005249319.2:c.14320G>A
|
XP_005249376.1:p.Ala4774Thr
|
|
XM_005249320.4:c.14299G>A
|
XP_005249377.1:p.Ala4767Thr
|
|
XM_005249322.5:c.14278G>A
|
XP_005249379.1:p.Ala4760Thr
|
|
XM_005249323.4:c.14200G>A
|
XP_005249380.1:p.Ala4734Thr
|
|
XM_005249324.3:c.13222G>A
|
XP_005249381.1:p.Ala4408Thr
|
|
XM_011514824.2:c.14761G>A
|
XP_011513126.1:p.Ala4921Thr
|
|
XM_011514825.3:c.8503G>A
|
XP_011513127.1:p.Ala2835Thr
|
|
XM_011514826.3:c.14200G>A
|
XP_011513128.1:p.Ala4734Thr
|
|
XM_017011205.1:c.14860G>A
|
XP_016866694.1:p.Ala4954Thr
|
|
XM_017011206.1:c.14860G>A
|
XP_016866695.1:p.Ala4954Thr
|
|
XM_017011207.1:c.14797G>A
|
XP_016866696.1:p.Ala4933Thr
|
|
XM_017011208.1:c.14860G>A
|
XP_016866697.1:p.Ala4954Thr
|
|
XM_017011209.1:c.14860G>A
|
XP_016866698.1:p.Ala4954Thr
|
|
XM_017011210.1:c.14860G>A
|
XP_016866699.1:p.Ala4954Thr
|
|
XM_017011211.2:c.14860G>A
|
XP_016866700.1:p.Ala4954Thr
|
|
XM_017011212.1:c.14626G>A
|
XP_016866701.1:p.Ala4876Thr
|
|
XM_017011213.1:c.14860G>A
|
XP_016866702.1:p.Ala4954Thr
|
|
XM_017011214.2:c.14860G>A
|
XP_016866703.1:p.Ala4954Thr
|
|
XM_017011215.2:c.14860G>A
|
XP_016866704.1:p.Ala4954Thr
|
|
XM_017011216.2:c.14860G>A
|
XP_016866705.1:p.Ala4954Thr
|
|
XM_017011217.1:c.14236G>A
|
XP_016866706.1:p.Ala4746Thr
|
|
XM_017011218.1:c.9427G>A
|
XP_016866707.1:p.Ala3143Thr
|
|
XM_017011219.1:c.8602G>A
|
XP_016866708.1:p.Ala2868Thr
|
|
XM_017011220.1:c.8476G>A
|
XP_016866709.1:p.Ala2826Thr
|
|
XM_017011221.1:c.8368G>A
|
XP_016866710.1:p.Ala2790Thr
|
|
XM_017011222.2:c.8290G>A
|
XP_016866711.1:p.Ala2764Thr
|
|
XM_017011223.1:c.8602G>A
|
XP_016866712.1:p.Ala2868Thr
|
|
XM_017011224.2:c.7942G>A
|
XP_016866713.1:p.Ala2648Thr
|
|
XM_024446530.1:c.14179G>A
|
XP_024302298.1:p.Ala4727Thr
|
|
NM_001144769.5:c.8476G>A
|
NP_001138241.1:p.Ala2826Thr
|
|
NM_001144770.2:c.8062G>A
|
NP_001138242.1:p.Ala2688Thr
|
|
NM_001374722.1:c.14833G>A
|
NP_001361651.1:p.Ala4945Thr
|
|
NM_001374729.1:c.14200G>A
|
NP_001361658.1:p.Ala4734Thr
|
|
NM_001374730.1:c.7942G>A
|
NP_001361659.1:p.Ala2648Thr
|
|
NM_001374734.1:c.14860G>A
|
NP_001361663.1:p.Ala4954Thr
|
|
NM_001374736.1:c.14833G>A
MANE Select
|
NP_001361665.1:p.Ala4945Thr
|
|
NM_015548.5:c.6964G>A
|
NP_056363.2:p.Ala2322Thr
|
|
NM_183380.4:c.7942G>A
|
NP_899236.1:p.Ala2648Thr
|
|
NM_001386100.1:c.7942G>A
|
NP_001373029.1:p.Ala2648Thr
|
|