|
ENST00000268704.7:c.2054G>A
|
ENSP00000268704.3:p.Ser685Asn
|
|
|
ENST00000561702.6:n.2747G>A
|
|
|
|
ENST00000566682.2:c.1116G>A
|
ENSP00000461979.2:n.1116G>A
|
|
|
ENST00000569720.2:n.758G>A
|
|
|
|
ENST00000569820.6:c.2348G>A
|
|
|
|
ENST00000642226.1:n.2138G>A
|
|
|
|
ENST00000642334.1:c.3493G>A
|
|
|
|
ENST00000642814.1:n.1490G>A
|
|
|
|
ENST00000642984.1:n.1798G>A
|
|
|
|
ENST00000643105.1:c.2781G>A
|
|
|
|
ENST00000643350.1:n.1489G>A
|
|
|
|
ENST00000643409.1:n.2500G>A
|
|
|
|
ENST00000643496.1:n.1892G>A
|
|
|
|
ENST00000643649.1:c.1964G>A
|
ENSP00000494806.1:p.Ser655Asn
|
|
|
ENST00000643668.1:c.*2369G>A
|
ENSP00000494903.1:n.*2369G>A
|
|
|
ENST00000643724.1:c.*1123G>A
|
ENSP00000496335.1:n.*1123G>A
|
|
|
ENST00000643954.1:c.2974G>A
|
|
|
|
ENST00000644171.1:n.2835G>A
|
|
|
|
ENST00000644210.1:c.*647G>A
|
ENSP00000495675.1:n.*647G>A
|
|
|
ENST00000644225.1:n.2092G>A
|
|
|
|
ENST00000644281.1:n.2759G>A
|
|
|
|
ENST00000644464.1:n.728G>A
|
|
|
|
ENST00000644498.1:c.*1894G>A
|
ENSP00000496244.1:n.*1894G>A
|
|
|
ENST00000644671.1:c.1732G>A
|
|
|
|
ENST00000644751.1:c.1263G>A
|
|
|
|
ENST00000644781.1:c.2030G>A
|
ENSP00000495473.1:p.Ser677Asn
|
|
|
ENST00000644901.1:c.*2469G>A
|
ENSP00000493797.1:n.*2469G>A
|
|
|
ENST00000645042.1:c.*849G>A
|
ENSP00000493908.1:n.*849G>A
|
|
|
ENST00000645063.1:c.2075G>A
|
ENSP00000493590.1:p.Ser692Asn
|
|
|
ENST00000645354.1:c.2835G>A
|
|
|
|
ENST00000645392.1:n.2416G>A
|
|
|
|
ENST00000645742.1:n.709G>A
|
|
|
|
ENST00000645818.2:c.2075G>A
MANE Select
|
ENSP00000495795.2:p.Ser692Asn
|
|
|
ENST00000645842.1:n.1920G>A
|
|
|
|
ENST00000645886.1:c.1580G>A
|
|
|
|
ENST00000645897.1:c.1613G>A
|
ENSP00000495293.1:p.Ser538Asn
|
|
|
ENST00000645952.1:n.1940G>A
|
|
|
|
ENST00000645977.1:n.3193G>A
|
|
|
|
ENST00000646005.1:n.1833G>A
|
|
|
|
ENST00000646263.1:c.*948G>A
|
ENSP00000494119.1:n.*948G>A
|
|
|
ENST00000646303.1:c.1943G>A
|
ENSP00000494160.1:p.Ser648Asn
|
|
|
ENST00000646399.1:c.2969G>A
|
|
|
|
ENST00000646445.1:c.933G>A
|
|
|
|
ENST00000646531.1:c.*698G>A
|
ENSP00000495185.1:n.*698G>A
|
|
|
ENST00000646589.1:c.*1203G>A
|
ENSP00000494739.1:n.*1203G>A
|
|
|
ENST00000646716.1:c.1127G>A
|
ENSP00000495593.1:p.Ser376Asn
|
|
|
ENST00000646826.1:c.*748G>A
|
ENSP00000495123.1:n.*748G>A
|
|
|
ENST00000646930.1:c.*2004G>A
|
ENSP00000495219.1:n.*2004G>A
|
|
|
ENST00000647032.1:c.1690G>A
|
|
|
|
ENST00000647079.1:c.1667G>A
|
ENSP00000495967.1:p.Ser556Asn
|
|
|
ENST00000647123.1:n.2032G>A
|
|
|
|
ENST00000647227.1:c.1713G>A
|
|
|
|
ENST00000647302.1:n.2725G>A
|
|
|
|
ENST00000647476.1:n.962G>A
|
|
|
|
ENST00000647491.1:n.1819G>A
|
|
|
|
ENST00000268704.6:c.2075G>A
|
ENSP00000268704.2:p.Ser692Asn
|
|
|
ENST00000561702.5:n.1060G>A
|
|
|
|
ENST00000561911.5:c.675G>A
|
ENSP00000457387.1:n.675G>A
|
|
|
ENST00000566682.1:c.211G>A
|
|
|
|
ENST00000569720.1:n.266G>A
|
|
|
|
ENST00000569820.5:c.1317G>A
|
|
|
|
ENST00000620811.4:c.*121G>A
|
ENSP00000478030.1:n.*121G>A
|
|
|
NM_003119.3:c.2075G>A
|
NP_003110.1:p.Ser692Asn
|
|
|
XM_006721264.2:c.2075G>A
|
XP_006721327.1:p.Ser692Asn
|
|
|
NM_001363850.1:c.2075G>A
|
NP_001350779.1:p.Ser692Asn
|
|
|
XM_006721264.4:c.2075G>A
|
XP_006721327.1:p.Ser692Asn
|
|
|
XR_001751971.2:n.2424G>A
|
|
|
|
XR_001751972.2:n.3711G>A
|
|
|
|
NM_003119.4:c.2075G>A
MANE Select
|
NP_003110.1:p.Ser692Asn
|
|
