|
ENST00000700029.2:c.754_755delinsAC
|
ENSP00000514759.2:p.Asp252Thr
|
|
|
ENST00000710265.1:c.754_755delinsAC
|
ENSP00000518161.1:p.Asp252Thr
|
|
|
ENST00000472832.3:c.754_755delinsAC
|
ENSP00000483066.2:p.Asp252Thr
|
|
|
ENST00000688158.2:n.1489_1490delinsAC
|
|
|
|
ENST00000688922.2:c.*584_*585delinsAC
|
ENSP00000508742.2:n.*584_*585delinsAC
|
|
|
ENST00000700021.1:c.709_710delinsAC
|
ENSP00000514757.1:p.Asp237Thr
|
|
|
ENST00000700022.1:c.*93_*94delinsAC
|
ENSP00000514758.1:n.*93_*94delinsAC
|
|
|
ENST00000700023.1:n.1912_1913delinsAC
|
|
|
|
ENST00000700024.1:n.2146_2147delinsAC
|
|
|
|
ENST00000700025.1:n.1523_1524delinsAC
|
|
|
|
ENST00000700026.1:n.391_392delinsAC
|
|
|
|
ENST00000700029.1:c.588_589delinsAC
|
|
|
|
ENST00000706954.1:c.754_755delinsAC
|
ENSP00000516674.1:p.Asp252Thr
|
|
|
ENST00000706955.1:c.*789_*790delinsAC
|
ENSP00000516675.1:n.*789_*790delinsAC
|
|
|
ENST00000686459.1:c.*340_*341delinsAC
|
ENSP00000508909.1:n.*340_*341delinsAC
|
|
|
ENST00000688158.1:c.*865_*866delinsAC
|
ENSP00000509254.1:n.*865_*866delinsAC
|
|
|
ENST00000688308.1:c.754_755delinsAC
|
ENSP00000508752.1:p.Asp252Thr
|
|
|
ENST00000688922.1:c.675_676delinsAC
|
|
|
|
ENST00000693560.1:c.1273_1274delinsAC
|
ENSP00000509861.1:p.Asp425Thr
|
|
|
ENST00000371953.8:c.754_755delinsAC
MANE Select
|
ENSP00000361021.3:p.Asp252Thr
|
|
|
ENST00000371953.7:c.754_755delinsAC
|
ENSP00000361021.3:p.Asp252Thr
|
|
|
ENST00000472832.2:c.181_182delinsAC
|
ENSP00000483066.1:p.Asp61Thr
|
|
|
NM_000314.5:c.754_755delinsAC
|
NP_000305.3:p.Asp252Thr
|
|
|
NM_000314.6:c.754_755delinsAC
|
NP_000305.3:p.Asp252Thr
|
|
|
NM_001304717.2:c.1273_1274delinsAC
|
NP_001291646.2:p.Asp425Thr
|
|
|
NM_001304718.1:c.163_164delinsAC
|
NP_001291647.1:p.Asp55Thr
|
|
|
XM_006717926.2:c.709_710delinsAC
|
XP_006717989.1:p.Asp237Thr
|
|
|
XM_011539981.1:c.754_755delinsAC
|
XP_011538283.1:p.Asp252Thr
|
|
|
XM_011539982.1:c.658_659delinsAC
|
XP_011538284.1:p.Asp220Thr
|
|
|
XR_945791.1:n.1324_1325delinsAC
|
|
|
|
NM_000314.7:c.754_755delinsAC
|
NP_000305.3:p.Asp252Thr
|
|
|
NM_001304717.5:c.1273_1274delinsAC
|
NP_001291646.4:p.Asp425Thr
|
|
|
NM_001304718.2:c.163_164delinsAC
|
NP_001291647.1:p.Asp55Thr
|
|
|
NM_000314.8:c.754_755delinsAC
MANE Select
|
NP_000305.3:p.Asp252Thr
|
|
