|
ENST00000700029.2:c.772_774delinsGCT
|
ENSP00000514759.2:p.Phe258Ala
|
|
|
ENST00000710265.1:c.772_774delinsGCT
|
ENSP00000518161.1:p.Phe258Ala
|
|
|
ENST00000472832.3:c.772_774delinsGCT
|
ENSP00000483066.2:p.Phe258Ala
|
|
|
ENST00000688158.2:n.1507_1509delinsGCT
|
|
|
|
ENST00000688922.2:c.*602_*604delinsGCT
|
ENSP00000508742.2:n.*602_*604delinsGCT
|
|
|
ENST00000700021.1:c.727_729delinsGCT
|
ENSP00000514757.1:p.Phe243Ala
|
|
|
ENST00000700022.1:c.*111_*113delinsGCT
|
ENSP00000514758.1:n.*111_*113delinsGCT
|
|
|
ENST00000700023.1:n.1930_1932delinsGCT
|
|
|
|
ENST00000700024.1:n.2164_2166delinsGCT
|
|
|
|
ENST00000700025.1:n.1541_1543delinsGCT
|
|
|
|
ENST00000700026.1:n.409_411delinsGCT
|
|
|
|
ENST00000700029.1:c.606_608delinsGCT
|
|
|
|
ENST00000706954.1:c.772_774delinsGCT
|
ENSP00000516674.1:p.Phe258Ala
|
|
|
ENST00000706955.1:c.*807_*809delinsGCT
|
ENSP00000516675.1:n.*807_*809delinsGCT
|
|
|
ENST00000686459.1:c.*358_*360delinsGCT
|
ENSP00000508909.1:n.*358_*360delinsGCT
|
|
|
ENST00000688158.1:c.*883_*885delinsGCT
|
ENSP00000509254.1:n.*883_*885delinsGCT
|
|
|
ENST00000688308.1:c.772_774delinsGCT
|
ENSP00000508752.1:p.Phe258Ala
|
|
|
ENST00000688922.1:c.693_695delinsGCT
|
|
|
|
ENST00000693560.1:c.1291_1293delinsGCT
|
ENSP00000509861.1:p.Phe431Ala
|
|
|
ENST00000371953.8:c.772_774delinsGCT
MANE Select
|
ENSP00000361021.3:p.Phe258Ala
|
|
|
ENST00000371953.7:c.772_774delinsGCT
|
ENSP00000361021.3:p.Phe258Ala
|
|
|
ENST00000472832.2:c.199_201delinsGCT
|
ENSP00000483066.1:p.Phe67Ala
|
|
|
NM_000314.5:c.772_774delinsGCT
|
NP_000305.3:p.Phe258Ala
|
|
|
NM_000314.6:c.772_774delinsGCT
|
NP_000305.3:p.Phe258Ala
|
|
|
NM_001304717.2:c.1291_1293delinsGCT
|
NP_001291646.2:p.Phe431Ala
|
|
|
NM_001304718.1:c.181_183delinsGCT
|
NP_001291647.1:p.Phe61Ala
|
|
|
XM_006717926.2:c.727_729delinsGCT
|
XP_006717989.1:p.Phe243Ala
|
|
|
XM_011539981.1:c.772_774delinsGCT
|
XP_011538283.1:p.Phe258Ala
|
|
|
XM_011539982.1:c.676_678delinsGCT
|
XP_011538284.1:p.Phe226Ala
|
|
|
XR_945791.1:n.1342_1344delinsGCT
|
|
|
|
NM_000314.7:c.772_774delinsGCT
|
NP_000305.3:p.Phe258Ala
|
|
|
NM_001304717.5:c.1291_1293delinsGCT
|
NP_001291646.4:p.Phe431Ala
|
|
|
NM_001304718.2:c.181_183delinsGCT
|
NP_001291647.1:p.Phe61Ala
|
|
|
NM_000314.8:c.772_774delinsGCT
MANE Select
|
NP_000305.3:p.Phe258Ala
|
|
