ENST00000505435.4:n.2975_2976delinsTG
|
|
|
ENST00000505787.8:n.3198_3199delinsTG
|
|
|
ENST00000509539.3:c.693_694delinsTG
|
ENSP00000425474.3:n.693_694delinsTG
|
|
ENST00000681968.1:c.860_861delinsTG
|
ENSP00000508143.1:p.Ala287Val
|
|
ENST00000681991.1:n.1451_1452delinsTG
|
|
|
ENST00000682045.1:c.1223_1224delinsTG
|
ENSP00000507329.1:p.Ala408Val
|
|
ENST00000682214.1:c.974_975delinsTG
|
ENSP00000507336.1:p.Ala325Val
|
|
ENST00000682231.1:n.385_386delinsTG
|
|
|
ENST00000682438.1:n.3366_3367delinsTG
|
|
|
ENST00000682499.1:n.2188_2189delinsTG
|
|
|
ENST00000682541.1:c.*265_*266delinsTG
|
ENSP00000507673.1:n.*265_*266delinsTG
|
|
ENST00000682640.1:n.1071_1072delinsTG
|
|
|
ENST00000682667.1:n.1559_1560delinsTG
|
|
|
ENST00000682687.1:c.*319_*320delinsTG
|
ENSP00000507945.1:n.*319_*320delinsTG
|
|
ENST00000682727.1:c.1358_1359delinsTG
|
ENSP00000507393.1:p.Ala453Val
|
|
ENST00000682876.1:c.1496_1497delinsTG
|
ENSP00000508389.1:p.Ala499Val
|
|
ENST00000683098.1:c.*55_*56delinsTG
|
ENSP00000507670.1:n.*55_*56delinsTG
|
|
ENST00000683258.1:c.*1088_*1089delinsTG
|
ENSP00000507448.1:n.*1088_*1089delinsTG
|
|
ENST00000683339.1:c.1151_1152delinsTG
|
ENSP00000507758.1:p.Ala384Val
|
|
ENST00000683403.1:c.1277_1278delinsTG
|
ENSP00000507896.1:p.Ala426Val
|
|
ENST00000683429.1:c.974_975delinsTG
|
ENSP00000507697.1:p.Ala325Val
|
|
ENST00000683789.1:c.1253_1254delinsTG
|
ENSP00000507012.1:p.Ala418Val
|
|
ENST00000683847.1:n.1537_1538delinsTG
|
|
|
ENST00000683882.1:c.*308_*309delinsTG
|
ENSP00000506735.1:n.*308_*309delinsTG
|
|
ENST00000684024.1:c.*1038_*1039delinsTG
|
ENSP00000507175.1:n.*1038_*1039delinsTG
|
|
ENST00000684132.1:c.295_296delinsTG
|
|
|
ENST00000684254.1:c.*1093_*1094delinsTG
|
ENSP00000508001.1:n.*1093_*1094delinsTG
|
|
ENST00000684310.1:c.533_534delinsTG
|
ENSP00000507550.1:p.Ala178Val
|
|
ENST00000684316.1:n.205_206delinsTG
|
|
|
ENST00000684474.1:n.1003_1004delinsTG
|
|
|
ENST00000684530.1:c.485_486delinsTG
|
ENSP00000507439.1:p.Ala162Val
|
|
ENST00000684686.1:n.986_987delinsTG
|
|
|
ENST00000340941.11:c.1367_1368delinsTG
MANE Select
|
ENSP00000343657.6:p.Ala456Val
|
|
ENST00000340941.10:c.1367_1368delinsTG
|
ENSP00000343657.6:p.Ala456Val
|
|
ENST00000509539.2:c.683_684delinsTG
|
ENSP00000425474.2:p.Ala228Val
|
|
ENST00000512218.6:c.*319_*320delinsTG
|
ENSP00000423202.2:n.*319_*320delinsTG
|
|
NM_022132.4:c.1367_1368delinsTG
|
NP_071415.1:p.Ala456Val
|
|
XM_005248567.1:c.1253_1254delinsTG
|
XP_005248624.1:p.Ala418Val
|
|
NM_001363147.1:c.1253_1254delinsTG
|
NP_001350076.1:p.Ala418Val
|
|
XR_001742172.1:n.1455_1456delinsTG
|
|
|
NM_022132.5:c.1367_1368delinsTG
MANE Select
|
NP_071415.1:p.Ala456Val
|
|