|
ENST00000700029.2:c.787_789delinsTCT
|
ENSP00000514759.2:p.Lys263Ser
|
|
|
ENST00000710265.1:c.787_789delinsTCT
|
ENSP00000518161.1:p.Lys263Ser
|
|
|
ENST00000472832.3:c.787_789delinsTCT
|
ENSP00000483066.2:p.Lys263Ser
|
|
|
ENST00000688158.2:n.1522_1524delinsTCT
|
|
|
|
ENST00000688922.2:c.*617_*619delinsTCT
|
ENSP00000508742.2:n.*617_*619delinsTCT
|
|
|
ENST00000700021.1:c.742_744delinsTCT
|
ENSP00000514757.1:p.Lys248Ser
|
|
|
ENST00000700022.1:c.*126_*128delinsTCT
|
ENSP00000514758.1:n.*126_*128delinsTCT
|
|
|
ENST00000700023.1:n.1945_1947delinsTCT
|
|
|
|
ENST00000700024.1:n.2179_2181delinsTCT
|
|
|
|
ENST00000700025.1:n.1556_1558delinsTCT
|
|
|
|
ENST00000700026.1:n.424_426delinsTCT
|
|
|
|
ENST00000700029.1:c.621_623delinsTCT
|
|
|
|
ENST00000706954.1:c.787_789delinsTCT
|
ENSP00000516674.1:p.Lys263Ser
|
|
|
ENST00000706955.1:c.*822_*824delinsTCT
|
ENSP00000516675.1:n.*822_*824delinsTCT
|
|
|
ENST00000686459.1:c.*373_*375delinsTCT
|
ENSP00000508909.1:n.*373_*375delinsTCT
|
|
|
ENST00000688158.1:c.*898_*900delinsTCT
|
ENSP00000509254.1:n.*898_*900delinsTCT
|
|
|
ENST00000688308.1:c.787_789delinsTCT
|
ENSP00000508752.1:p.Lys263Ser
|
|
|
ENST00000688922.1:c.708_710delinsTCT
|
|
|
|
ENST00000693560.1:c.1306_1308delinsTCT
|
ENSP00000509861.1:p.Lys436Ser
|
|
|
ENST00000371953.8:c.787_789delinsTCT
MANE Select
|
ENSP00000361021.3:p.Lys263Ser
|
|
|
ENST00000371953.7:c.787_789delinsTCT
|
ENSP00000361021.3:p.Lys263Ser
|
|
|
ENST00000472832.2:c.214_216delinsTCT
|
ENSP00000483066.1:p.Lys72Ser
|
|
|
NM_000314.5:c.787_789delinsTCT
|
NP_000305.3:p.Lys263Ser
|
|
|
NM_000314.6:c.787_789delinsTCT
|
NP_000305.3:p.Lys263Ser
|
|
|
NM_001304717.2:c.1306_1308delinsTCT
|
NP_001291646.2:p.Lys436Ser
|
|
|
NM_001304718.1:c.196_198delinsTCT
|
NP_001291647.1:p.Lys66Ser
|
|
|
XM_006717926.2:c.742_744delinsTCT
|
XP_006717989.1:p.Lys248Ser
|
|
|
XM_011539981.1:c.787_789delinsTCT
|
XP_011538283.1:p.Lys263Ser
|
|
|
XM_011539982.1:c.691_693delinsTCT
|
XP_011538284.1:p.Lys231Ser
|
|
|
XR_945791.1:n.1357_1359delinsTCT
|
|
|
|
NM_000314.7:c.787_789delinsTCT
|
NP_000305.3:p.Lys263Ser
|
|
|
NM_001304717.5:c.1306_1308delinsTCT
|
NP_001291646.4:p.Lys436Ser
|
|
|
NM_001304718.2:c.196_198delinsTCT
|
NP_001291647.1:p.Lys66Ser
|
|
|
NM_000314.8:c.787_789delinsTCT
MANE Select
|
NP_000305.3:p.Lys263Ser
|
|
