ENST00000421834.7:c.7837G>T
|
ENSP00000400883.3:p.Asp2613Tyr
|
|
ENST00000449297.7:c.8371G>T
|
ENSP00000393082.3:p.Asp2791Tyr
|
|
ENST00000520645.6:c.7957G>T
|
ENSP00000431030.2:p.Asp2653Tyr
|
|
ENST00000520144.2:n.699G>T
|
|
|
ENST00000680361.1:c.14728G>T
MANE Select
|
ENSP00000505098.1:p.Asp4910Tyr
|
|
ENST00000244364.10:c.6859G>T
|
ENSP00000244364.6:p.Asp2287Tyr
|
|
ENST00000312431.10:c.7957G>T
|
ENSP00000307959.7:p.Asp2653Tyr
|
|
ENST00000361203.7:c.14095G>T
|
ENSP00000354508.3:p.Asp4699Tyr
|
|
ENST00000370754.9:c.8371G>T
|
ENSP00000359790.6:p.Asp2791Tyr
|
|
ENST00000370788.6:c.7837G>T
|
ENSP00000359824.2:p.Asp2613Tyr
|
|
ENST00000421834.6:c.7837G>T
|
ENSP00000400883.3:p.Asp2613Tyr
|
|
ENST00000520144.1:n.437G>T
|
|
|
NM_001144769.2:c.8371G>T
|
NP_001138241.1:p.Asp2791Tyr
|
|
NM_001144770.1:c.7957G>T
|
NP_001138242.1:p.Asp2653Tyr
|
|
NM_015548.4:c.6859G>T
|
NP_056363.2:p.Asp2287Tyr
|
|
NM_183380.3:c.7837G>T
|
NP_899236.1:p.Asp2613Tyr
|
|
XM_005249310.2:c.14728G>T
|
XP_005249367.1:p.Asp4910Tyr
|
|
XM_005249315.2:c.14629G>T
|
XP_005249372.1:p.Asp4877Tyr
|
|
XM_005249316.1:c.14443G>T
|
XP_005249373.1:p.Asp4815Tyr
|
|
XM_005249318.1:c.14314G>T
|
XP_005249375.1:p.Asp4772Tyr
|
|
XM_005249319.1:c.14215G>T
|
XP_005249376.1:p.Asp4739Tyr
|
|
XM_005249320.3:c.14194G>T
|
XP_005249377.1:p.Asp4732Tyr
|
|
XM_005249322.3:c.14173G>T
|
XP_005249379.1:p.Asp4725Tyr
|
|
XM_005249323.2:c.14095G>T
|
XP_005249380.1:p.Asp4699Tyr
|
|
XM_005249324.1:c.13117G>T
|
XP_005249381.1:p.Asp4373Tyr
|
|
XM_011514824.1:c.14656G>T
|
XP_011513126.1:p.Asp4886Tyr
|
|
XM_011514825.1:c.8398G>T
|
XP_011513127.1:p.Asp2800Tyr
|
|
XM_011514826.1:c.14095G>T
|
XP_011513128.1:p.Asp4699Tyr
|
|
XM_005249310.4:c.14728G>T
|
XP_005249367.1:p.Asp4910Tyr
|
|
XM_005249315.3:c.14629G>T
|
XP_005249372.1:p.Asp4877Tyr
|
|
XM_005249316.3:c.14443G>T
|
XP_005249373.1:p.Asp4815Tyr
|
|
XM_005249318.2:c.14314G>T
|
XP_005249375.1:p.Asp4772Tyr
|
|
XM_005249319.2:c.14215G>T
|
XP_005249376.1:p.Asp4739Tyr
|
|
XM_005249320.4:c.14194G>T
|
XP_005249377.1:p.Asp4732Tyr
|
|
XM_005249322.5:c.14173G>T
|
XP_005249379.1:p.Asp4725Tyr
|
|
XM_005249323.4:c.14095G>T
|
XP_005249380.1:p.Asp4699Tyr
|
|
XM_005249324.3:c.13117G>T
|
XP_005249381.1:p.Asp4373Tyr
|
|
XM_011514824.2:c.14656G>T
|
XP_011513126.1:p.Asp4886Tyr
|
|
XM_011514825.3:c.8398G>T
|
XP_011513127.1:p.Asp2800Tyr
|
|
XM_011514826.3:c.14095G>T
|
XP_011513128.1:p.Asp4699Tyr
|
|
XM_017011205.1:c.14755G>T
|
XP_016866694.1:p.Asp4919Tyr
|
|
XM_017011206.1:c.14755G>T
|
XP_016866695.1:p.Asp4919Tyr
|
|
XM_017011207.1:c.14692G>T
|
XP_016866696.1:p.Asp4898Tyr
|
|
XM_017011208.1:c.14755G>T
|
XP_016866697.1:p.Asp4919Tyr
|
|
XM_017011209.1:c.14755G>T
|
XP_016866698.1:p.Asp4919Tyr
|
|
XM_017011210.1:c.14755G>T
|
XP_016866699.1:p.Asp4919Tyr
|
|
XM_017011211.2:c.14755G>T
|
XP_016866700.1:p.Asp4919Tyr
|
|
XM_017011212.1:c.14521G>T
|
XP_016866701.1:p.Asp4841Tyr
|
|
XM_017011213.1:c.14755G>T
|
XP_016866702.1:p.Asp4919Tyr
|
|
XM_017011214.2:c.14755G>T
|
XP_016866703.1:p.Asp4919Tyr
|
|
XM_017011215.2:c.14755G>T
|
XP_016866704.1:p.Asp4919Tyr
|
|
XM_017011216.2:c.14755G>T
|
XP_016866705.1:p.Asp4919Tyr
|
|
XM_017011217.1:c.14131G>T
|
XP_016866706.1:p.Asp4711Tyr
|
|
XM_017011218.1:c.9322G>T
|
XP_016866707.1:p.Asp3108Tyr
|
|
XM_017011219.1:c.8497G>T
|
XP_016866708.1:p.Asp2833Tyr
|
|
XM_017011220.1:c.8371G>T
|
XP_016866709.1:p.Asp2791Tyr
|
|
XM_017011221.1:c.8263G>T
|
XP_016866710.1:p.Asp2755Tyr
|
|
XM_017011222.2:c.8185G>T
|
XP_016866711.1:p.Asp2729Tyr
|
|
XM_017011223.1:c.8497G>T
|
XP_016866712.1:p.Asp2833Tyr
|
|
XM_017011224.2:c.7837G>T
|
XP_016866713.1:p.Asp2613Tyr
|
|
XM_024446530.1:c.14074G>T
|
XP_024302298.1:p.Asp4692Tyr
|
|
NM_001144769.5:c.8371G>T
|
NP_001138241.1:p.Asp2791Tyr
|
|
NM_001144770.2:c.7957G>T
|
NP_001138242.1:p.Asp2653Tyr
|
|
NM_001374722.1:c.14728G>T
|
NP_001361651.1:p.Asp4910Tyr
|
|
NM_001374729.1:c.14095G>T
|
NP_001361658.1:p.Asp4699Tyr
|
|
NM_001374730.1:c.7837G>T
|
NP_001361659.1:p.Asp2613Tyr
|
|
NM_001374734.1:c.14755G>T
|
NP_001361663.1:p.Asp4919Tyr
|
|
NM_001374736.1:c.14728G>T
MANE Select
|
NP_001361665.1:p.Asp4910Tyr
|
|
NM_015548.5:c.6859G>T
|
NP_056363.2:p.Asp2287Tyr
|
|
NM_183380.4:c.7837G>T
|
NP_899236.1:p.Asp2613Tyr
|
|
NM_001386100.1:c.7837G>T
|
NP_001373029.1:p.Asp2613Tyr
|
|