|
ENST00000310638.9:c.1364+335_1364+341delinsACTTCAG
MANE Select
|
ENSP00000311095.4:n.1364+335_1364+341delinsACTTCAG
|
|
|
ENST00000310638.8:c.1364+335_1364+341delinsACTTCAG
|
ENSP00000311095.4:n.1364+335_1364+341delinsACTTCAG
|
|
|
ENST00000371904.8:c.1367+335_1367+341delinsACTTCAG
|
ENSP00000360971.4:n.1367+335_1367+341delinsACTTCAG
|
|
|
ENST00000462347.5:c.1070+335_1070+341delinsACTTCAG
|
ENSP00000477495.1:n.1070+335_1070+341delinsACTTCAG
|
|
|
ENST00000465874.5:c.*497_*503delinsACTTCAG
|
ENSP00000476368.1:n.*497_*503delinsACTTCAG
|
|
|
ENST00000468629.5:c.*69+335_*69+341delinsACTTCAG
|
ENSP00000476619.1:n.*69+335_*69+341delinsACTTCAG
|
|
|
ENST00000474458.5:c.*69+335_*69+341delinsACTTCAG
|
ENSP00000476988.1:n.*69+335_*69+341delinsACTTCAG
|
|
|
ENST00000475477.5:c.*158+335_*158+341delinsACTTCAG
|
ENSP00000476854.1:n.*158+335_*158+341delinsACTTCAG
|
|
|
NM_000778.3:c.1364+335_1364+341delinsACTTCAG
|
NP_000769.2:n.1364+335_1364+341delinsACTTCAG
|
|
|
XM_011540826.1:c.1382+335_1382+341delinsACTTCAG
|
XP_011539128.1:n.1382+335_1382+341delinsACTTCAG
|
|
|
XM_011540827.1:c.1088+335_1088+341delinsACTTCAG
|
XP_011539129.1:n.1088+335_1088+341delinsACTTCAG
|
|
|
XM_011540828.1:c.1070+335_1070+341delinsACTTCAG
|
XP_011539130.1:n.1070+335_1070+341delinsACTTCAG
|
|
|
XR_246241.1:n.1268+335_1268+341delinsACTTCAG
|
|
|
|
XR_246242.1:n.1252+335_1252+341delinsACTTCAG
|
|
|
|
NM_001319155.1:c.1268+335_1268+341delinsACTTCAG
|
NP_001306084.1:n.1268+335_1268+341delinsACTTCAG
|
|
|
NM_001363587.1:c.1070+335_1070+341delinsACTTCAG
|
NP_001350516.1:n.1070+335_1070+341delinsACTTCAG
|
|
|
NR_134988.1:n.1069+335_1069+341delinsACTTCAG
|
|
|
|
NR_134989.1:n.1260+335_1260+341delinsACTTCAG
|
|
|
|
NR_134990.1:n.1254+335_1254+341delinsACTTCAG
|
|
|
|
NR_134991.1:n.1241+335_1241+341delinsACTTCAG
|
|
|
|
NR_134992.1:n.870+335_870+341delinsACTTCAG
|
|
|
|
NR_134993.1:n.1004+335_1004+341delinsACTTCAG
|
|
|
|
NR_134994.1:n.1276+335_1276+341delinsACTTCAG
|
|
|
|
XM_017000465.1:c.1052+335_1052+341delinsACTTCAG
|
XP_016855954.1:n.1052+335_1052+341delinsACTTCAG
|
|
|
XR_001737005.1:n.1342+335_1342+341delinsACTTCAG
|
|
|
|
NM_000778.4:c.1364+335_1364+341delinsACTTCAG
MANE Select
|
NP_000769.2:n.1364+335_1364+341delinsACTTCAG
|
|
|
NM_001319155.2:c.1268+335_1268+341delinsACTTCAG
|
NP_001306084.1:n.1268+335_1268+341delinsACTTCAG
|
|
|
NM_001363587.2:c.1070+335_1070+341delinsACTTCAG
|
NP_001350516.1:n.1070+335_1070+341delinsACTTCAG
|
|
|
NR_134988.2:n.1061+335_1061+341delinsACTTCAG
|
|
|
|
NR_134989.2:n.1252+335_1252+341delinsACTTCAG
|
|
|
|
NR_134990.2:n.1246+335_1246+341delinsACTTCAG
|
|
|
|
NR_134991.2:n.1233+335_1233+341delinsACTTCAG
|
|
|
|
NR_134992.2:n.862+335_862+341delinsACTTCAG
|
|
|
|
NR_134993.2:n.996+335_996+341delinsACTTCAG
|
|
|
|
NR_134994.2:n.1268+335_1268+341delinsACTTCAG
|
|
|
