ENST00000700029.2:c.691_693delinsTCT
|
ENSP00000514759.2:p.Pro231Ser
|
|
ENST00000710265.1:c.691_693delinsTCT
|
ENSP00000518161.1:p.Pro231Ser
|
|
ENST00000472832.3:c.691_693delinsTCT
|
ENSP00000483066.2:p.Pro231Ser
|
|
ENST00000688158.2:n.1426_1428delinsTCT
|
|
|
ENST00000688922.2:c.*521_*523delinsTCT
|
ENSP00000508742.2:n.*521_*523delinsTCT
|
|
ENST00000700021.1:c.646_648delinsTCT
|
ENSP00000514757.1:p.Pro216Ser
|
|
ENST00000700022.1:c.*30_*32delinsTCT
|
ENSP00000514758.1:n.*30_*32delinsTCT
|
|
ENST00000700023.1:n.1849_1851delinsTCT
|
|
|
ENST00000700024.1:n.2083_2085delinsTCT
|
|
|
ENST00000700025.1:n.1460_1462delinsTCT
|
|
|
ENST00000700026.1:n.328_330delinsTCT
|
|
|
ENST00000700029.1:c.525_527delinsTCT
|
|
|
ENST00000706954.1:c.691_693delinsTCT
|
ENSP00000516674.1:p.Pro231Ser
|
|
ENST00000706955.1:c.*726_*728delinsTCT
|
ENSP00000516675.1:n.*726_*728delinsTCT
|
|
ENST00000686459.1:c.*277_*279delinsTCT
|
ENSP00000508909.1:n.*277_*279delinsTCT
|
|
ENST00000688158.1:c.*802_*804delinsTCT
|
ENSP00000509254.1:n.*802_*804delinsTCT
|
|
ENST00000688308.1:c.691_693delinsTCT
|
ENSP00000508752.1:p.Pro231Ser
|
|
ENST00000688922.1:c.612_614delinsTCT
|
|
|
ENST00000693560.1:c.1210_1212delinsTCT
|
ENSP00000509861.1:p.Pro404Ser
|
|
ENST00000371953.8:c.691_693delinsTCT
MANE Select
|
ENSP00000361021.3:p.Pro231Ser
|
|
ENST00000371953.7:c.691_693delinsTCT
|
ENSP00000361021.3:p.Pro231Ser
|
|
ENST00000472832.2:c.118_120delinsTCT
|
ENSP00000483066.1:p.Pro40Ser
|
|
NM_000314.5:c.691_693delinsTCT
|
NP_000305.3:p.Pro231Ser
|
|
NM_000314.6:c.691_693delinsTCT
|
NP_000305.3:p.Pro231Ser
|
|
NM_001304717.2:c.1210_1212delinsTCT
|
NP_001291646.2:p.Pro404Ser
|
|
NM_001304718.1:c.100_102delinsTCT
|
NP_001291647.1:p.Pro34Ser
|
|
XM_006717926.2:c.646_648delinsTCT
|
XP_006717989.1:p.Pro216Ser
|
|
XM_011539981.1:c.691_693delinsTCT
|
XP_011538283.1:p.Pro231Ser
|
|
XM_011539982.1:c.595_597delinsTCT
|
XP_011538284.1:p.Pro199Ser
|
|
XR_945791.1:n.1261_1263delinsTCT
|
|
|
NM_000314.7:c.691_693delinsTCT
|
NP_000305.3:p.Pro231Ser
|
|
NM_001304717.5:c.1210_1212delinsTCT
|
NP_001291646.4:p.Pro404Ser
|
|
NM_001304718.2:c.100_102delinsTCT
|
NP_001291647.1:p.Pro34Ser
|
|
NM_000314.8:c.691_693delinsTCT
MANE Select
|
NP_000305.3:p.Pro231Ser
|
|