|
ENST00000700029.2:c.787_789delinsTAT
|
ENSP00000514759.2:p.Lys263Tyr
|
|
|
ENST00000710265.1:c.787_789delinsTAT
|
ENSP00000518161.1:p.Lys263Tyr
|
|
|
ENST00000472832.3:c.787_789delinsTAT
|
ENSP00000483066.2:p.Lys263Tyr
|
|
|
ENST00000688158.2:n.1522_1524delinsTAT
|
|
|
|
ENST00000688922.2:c.*617_*619delinsTAT
|
ENSP00000508742.2:n.*617_*619delinsTAT
|
|
|
ENST00000700021.1:c.742_744delinsTAT
|
ENSP00000514757.1:p.Lys248Tyr
|
|
|
ENST00000700022.1:c.*126_*128delinsTAT
|
ENSP00000514758.1:n.*126_*128delinsTAT
|
|
|
ENST00000700023.1:n.1945_1947delinsTAT
|
|
|
|
ENST00000700024.1:n.2179_2181delinsTAT
|
|
|
|
ENST00000700025.1:n.1556_1558delinsTAT
|
|
|
|
ENST00000700026.1:n.424_426delinsTAT
|
|
|
|
ENST00000700029.1:c.621_623delinsTAT
|
|
|
|
ENST00000706954.1:c.787_789delinsTAT
|
ENSP00000516674.1:p.Lys263Tyr
|
|
|
ENST00000706955.1:c.*822_*824delinsTAT
|
ENSP00000516675.1:n.*822_*824delinsTAT
|
|
|
ENST00000686459.1:c.*373_*375delinsTAT
|
ENSP00000508909.1:n.*373_*375delinsTAT
|
|
|
ENST00000688158.1:c.*898_*900delinsTAT
|
ENSP00000509254.1:n.*898_*900delinsTAT
|
|
|
ENST00000688308.1:c.787_789delinsTAT
|
ENSP00000508752.1:p.Lys263Tyr
|
|
|
ENST00000688922.1:c.708_710delinsTAT
|
|
|
|
ENST00000693560.1:c.1306_1308delinsTAT
|
ENSP00000509861.1:p.Lys436Tyr
|
|
|
ENST00000371953.8:c.787_789delinsTAT
MANE Select
|
ENSP00000361021.3:p.Lys263Tyr
|
|
|
ENST00000371953.7:c.787_789delinsTAT
|
ENSP00000361021.3:p.Lys263Tyr
|
|
|
ENST00000472832.2:c.214_216delinsTAT
|
ENSP00000483066.1:p.Lys72Tyr
|
|
|
NM_000314.5:c.787_789delinsTAT
|
NP_000305.3:p.Lys263Tyr
|
|
|
NM_000314.6:c.787_789delinsTAT
|
NP_000305.3:p.Lys263Tyr
|
|
|
NM_001304717.2:c.1306_1308delinsTAT
|
NP_001291646.2:p.Lys436Tyr
|
|
|
NM_001304718.1:c.196_198delinsTAT
|
NP_001291647.1:p.Lys66Tyr
|
|
|
XM_006717926.2:c.742_744delinsTAT
|
XP_006717989.1:p.Lys248Tyr
|
|
|
XM_011539981.1:c.787_789delinsTAT
|
XP_011538283.1:p.Lys263Tyr
|
|
|
XM_011539982.1:c.691_693delinsTAT
|
XP_011538284.1:p.Lys231Tyr
|
|
|
XR_945791.1:n.1357_1359delinsTAT
|
|
|
|
NM_000314.7:c.787_789delinsTAT
|
NP_000305.3:p.Lys263Tyr
|
|
|
NM_001304717.5:c.1306_1308delinsTAT
|
NP_001291646.4:p.Lys436Tyr
|
|
|
NM_001304718.2:c.196_198delinsTAT
|
NP_001291647.1:p.Lys66Tyr
|
|
|
NM_000314.8:c.787_789delinsTAT
MANE Select
|
NP_000305.3:p.Lys263Tyr
|
|
