ENST00000350026.11:c.3074A>C
|
ENSP00000055163.8:p.Asn1025Thr
|
|
ENST00000414678.8:c.2984A>C
|
ENSP00000412835.3:p.Asn995Thr
|
|
ENST00000637015.2:c.3074A>C
|
ENSP00000489729.2:p.Asn1025Thr
|
|
ENST00000319584.11:c.1088A>C
|
ENSP00000313006.7:p.Asn363Thr
|
|
ENST00000346085.10:c.3113A>C
|
ENSP00000344546.5:p.Asn1038Thr
|
|
ENST00000350026.10:c.2825A>C
|
ENSP00000055163.7:p.Asn942Thr
|
|
ENST00000414678.7:c.1232A>C
|
ENSP00000412835.2:p.Asn411Thr
|
|
ENST00000452544.2:n.975A>C
|
|
|
ENST00000635849.1:c.395A>C
|
ENSP00000490948.1:p.Asn132Thr
|
|
ENST00000635957.1:c.29A>C
|
ENSP00000490385.1:p.Asn10Thr
|
|
ENST00000636426.1:n.208A>C
|
|
|
ENST00000636930.2:c.3074A>C
MANE Select
|
ENSP00000490491.2:p.Asn1025Thr
|
|
ENST00000637015.1:c.313A>C
|
|
|
ENST00000637568.1:c.117A>C
|
|
|
ENST00000637810.1:c.575A>C
|
ENSP00000489636.1:p.Asn192Thr
|
|
ENST00000637904.1:c.575A>C
|
ENSP00000490550.1:p.Asn192Thr
|
|
ENST00000647938.1:c.2864A>C
|
ENSP00000498155.1:p.Asn955Thr
|
|
ENST00000674190.1:n.1823A>C
|
|
|
ENST00000319584.10:c.1091A>C
|
ENSP00000313006.6:p.Asn364Thr
|
|
ENST00000346085.9:c.2864A>C
|
ENSP00000344546.4:p.Asn955Thr
|
|
ENST00000350026.9:c.2825A>C
|
ENSP00000055163.7:p.Asn942Thr
|
|
ENST00000400790.3:c.26A>C
|
ENSP00000383596.3:p.Asn9Thr
|
|
ENST00000414678.6:c.1232A>C
|
ENSP00000412835.2:p.Asn411Thr
|
|
ENST00000452544.1:n.921A>C
|
|
|
ENST00000478761.3:c.147A>C
|
|
|
NM_017519.2:c.2825A>C
|
NP_059989.2:p.Asn942Thr
|
|
NM_020732.3:c.2864A>C
|
NP_065783.3:p.Asn955Thr
|
|
XM_005267069.3:c.2825A>C
|
XP_005267126.2:p.Asn942Thr
|
|
XM_011535984.1:c.1775A>C
|
XP_011534286.1:p.Asn592Thr
|
|
XM_011535985.1:c.1595A>C
|
XP_011534287.1:p.Asn532Thr
|
|
XM_011535986.1:c.1355A>C
|
XP_011534288.1:p.Asn452Thr
|
|
XM_011535987.1:c.974A>C
|
XP_011534289.1:p.Asn325Thr
|
|
XM_011535988.1:c.-20+15729A>C
|
XP_011534290.1:n.-20+15729A>C
|
|
NM_001346813.1:c.2825A>C
|
NP_001333742.1:p.Asn942Thr
|
|
NM_001363725.1:c.575A>C
|
NP_001350654.1:p.Asn192Thr
|
|
XM_011535984.2:c.2906A>C
|
XP_011534286.2:p.Asn969Thr
|
|
XM_011535988.3:c.-20+15729A>C
|
XP_011534290.1:n.-20+15729A>C
|
|
XM_017011103.2:c.2906A>C
|
XP_016866592.1:p.Asn969Thr
|
|
XM_017011104.1:c.2906A>C
|
XP_016866593.1:p.Asn969Thr
|
|
XM_017011105.2:c.2906A>C
|
XP_016866594.1:p.Asn969Thr
|
|
XM_017011106.2:c.2906A>C
|
XP_016866595.1:p.Asn969Thr
|
|
XM_017011107.2:c.2726A>C
|
XP_016866596.1:p.Asn909Thr
|
|
XR_002956289.1:n.2989A>C
|
|
|
NM_001363725.2:c.575A>C
|
NP_001350654.1:p.Asn192Thr
|
|
NM_001371656.1:c.3113A>C
|
NP_001358585.1:p.Asn1038Thr
|
|
NM_001374820.1:c.3113A>C
|
NP_001361749.1:p.Asn1038Thr
|
|
NM_001374828.1:c.3074A>C
MANE Select
|
NP_001361757.1:p.Asn1025Thr
|
|
NM_017519.3:c.3074A>C
|
NP_059989.3:p.Asn1025Thr
|
|