|
ENST00000347147.9:c.1018-193_1018-192insTGTATCCCTCC
MANE Select
|
ENSP00000333355.6:n.1018-193_1018-192insTGTATCCCTCC
|
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ENST00000347147.8:c.1018-193_1018-192insTGTATCCCTCC
|
ENSP00000333355.6:n.1018-193_1018-192insTGTATCCCTCC
|
|
|
ENST00000381975.7:c.1018-197_1018-196insTGTATCCCTCC
|
ENSP00000371402.3:n.1018-197_1018-196insTGTATCCCTCC
|
|
|
ENST00000392432.6:c.1159-193_1159-192insTGTATCCCTCC
|
ENSP00000376227.2:n.1159-193_1159-192insTGTATCCCTCC
|
|
|
ENST00000419280.5:c.*314-193_*314-192insTGTATCCCTCC
|
ENSP00000414077.1:n.*314-193_*314-192insTGTATCCCTCC
|
|
|
ENST00000429560.1:c.214-197_214-196insTGTATCCCTCC
|
ENSP00000403053.1:n.214-197_214-196insTGTATCCCTCC
|
|
|
ENST00000432352.5:c.292-193_292-192insTGTATCCCTCC
|
ENSP00000409963.1:n.292-193_292-192insTGTATCCCTCC
|
|
|
ENST00000452358.5:c.517-193_517-192insTGTATCCCTCC
|
ENSP00000414333.1:n.517-193_517-192insTGTATCCCTCC
|
|
|
ENST00000467284.1:n.64-193_64-192insTGTATCCCTCC
|
|
|
|
ENST00000473092.5:c.1018-193_1018-192insTGTATCCCTCC
|
ENSP00000418674.1:n.1018-193_1018-192insTGTATCCCTCC
|
|
|
ENST00000477651.5:n.782-193_782-192insTGTATCCCTCC
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|
|
|
NM_001011655.2:c.1018-193_1018-192insTGTATCCCTCC
|
NP_001011655.1:n.1018-193_1018-192insTGTATCCCTCC
|
|
|
NM_001166305.1:c.1159-193_1159-192insTGTATCCCTCC
|
NP_001159777.1:n.1159-193_1159-192insTGTATCCCTCC
|
|
|
NM_001166306.1:c.1018-197_1018-196insTGTATCCCTCC
|
NP_001159778.1:n.1018-197_1018-196insTGTATCCCTCC
|
|
|
NM_138399.4:c.1018-193_1018-192insTGTATCCCTCC
|
NP_612408.3:n.1018-193_1018-192insTGTATCCCTCC
|
|
|
XM_005269371.3:c.1018-193_1018-192insTGTATCCCTCC
|
XP_005269428.1:n.1018-193_1018-192insTGTATCCCTCC
|
|
|
XM_011513318.1:c.1168-193_1168-192insTGTATCCCTCC
|
XP_011511620.1:n.1168-193_1168-192insTGTATCCCTCC
|
|
|
XM_011513319.1:c.1105-193_1105-192insTGTATCCCTCC
|
XP_011511621.1:n.1105-193_1105-192insTGTATCCCTCC
|
|
|
XM_011513320.1:c.1216-193_1216-192insTGTATCCCTCC
|
XP_011511622.1:n.1216-193_1216-192insTGTATCCCTCC
|
|
|
XM_011513321.1:c.1084-193_1084-192insTGTATCCCTCC
|
XP_011511623.1:n.1084-193_1084-192insTGTATCCCTCC
|
|
|
XM_011513322.1:c.1075-193_1075-192insTGTATCCCTCC
|
XP_011511624.1:n.1075-193_1075-192insTGTATCCCTCC
|
|
|
XM_011513323.1:c.913-193_913-192insTGTATCCCTCC
|
XP_011511625.1:n.913-193_913-192insTGTATCCCTCC
|
|
|
XM_005269371.4:c.1018-193_1018-192insTGTATCCCTCC
|
XP_005269428.1:n.1018-193_1018-192insTGTATCCCTCC
|
|
|
XM_011513318.2:c.1168-193_1168-192insTGTATCCCTCC
|
XP_011511620.1:n.1168-193_1168-192insTGTATCCCTCC
|
|
|
XM_011513319.2:c.1105-193_1105-192insTGTATCCCTCC
|
XP_011511621.1:n.1105-193_1105-192insTGTATCCCTCC
|
|
|
XM_011513320.2:c.1216-193_1216-192insTGTATCCCTCC
|
XP_011511622.1:n.1216-193_1216-192insTGTATCCCTCC
|
|
|
XM_011513321.2:c.1084-193_1084-192insTGTATCCCTCC
|
XP_011511623.1:n.1084-193_1084-192insTGTATCCCTCC
|
|
|
XM_011513322.2:c.1075-193_1075-192insTGTATCCCTCC
|
XP_011511624.1:n.1075-193_1075-192insTGTATCCCTCC
|
|
|
XM_017007517.1:c.1027-193_1027-192insTGTATCCCTCC
|
XP_016863006.1:n.1027-193_1027-192insTGTATCCCTCC
|
|
|
XM_017007518.1:c.1027-193_1027-192insTGTATCCCTCC
|
XP_016863007.1:n.1027-193_1027-192insTGTATCCCTCC
|
|
|
NM_001011655.3:c.1018-193_1018-192insTGTATCCCTCC
MANE Select
|
NP_001011655.1:n.1018-193_1018-192insTGTATCCCTCC
|
|
|
NM_001166305.2:c.1159-193_1159-192insTGTATCCCTCC
|
NP_001159777.1:n.1159-193_1159-192insTGTATCCCTCC
|
|
|
NM_001166306.2:c.1018-197_1018-196insTGTATCCCTCC
|
NP_001159778.1:n.1018-197_1018-196insTGTATCCCTCC
|
|
|
NM_138399.5:c.1018-193_1018-192insTGTATCCCTCC
|
NP_612408.3:n.1018-193_1018-192insTGTATCCCTCC
|
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