|
ENST00000700029.2:c.757A>T
|
ENSP00000514759.2:p.Ile253Phe
|
|
|
ENST00000710265.1:c.757A>T
|
ENSP00000518161.1:p.Ile253Phe
|
|
|
ENST00000472832.3:c.757A>T
|
ENSP00000483066.2:p.Ile253Phe
|
|
|
ENST00000688158.2:n.1492A>T
|
|
|
|
ENST00000688922.2:c.*587A>T
|
ENSP00000508742.2:n.*587A>T
|
|
|
ENST00000700021.1:c.712A>T
|
ENSP00000514757.1:p.Ile238Phe
|
|
|
ENST00000700022.1:c.*96A>T
|
ENSP00000514758.1:n.*96A>T
|
|
|
ENST00000700023.1:n.1915A>T
|
|
|
|
ENST00000700024.1:n.2149A>T
|
|
|
|
ENST00000700025.1:n.1526A>T
|
|
|
|
ENST00000700026.1:n.394A>T
|
|
|
|
ENST00000700029.1:c.591A>T
|
|
|
|
ENST00000706954.1:c.757A>T
|
ENSP00000516674.1:p.Ile253Phe
|
|
|
ENST00000706955.1:c.*792A>T
|
ENSP00000516675.1:n.*792A>T
|
|
|
ENST00000686459.1:c.*343A>T
|
ENSP00000508909.1:n.*343A>T
|
|
|
ENST00000688158.1:c.*868A>T
|
ENSP00000509254.1:n.*868A>T
|
|
|
ENST00000688308.1:c.757A>T
|
ENSP00000508752.1:p.Ile253Phe
|
|
|
ENST00000688922.1:c.678A>T
|
|
|
|
ENST00000693560.1:c.1276A>T
|
ENSP00000509861.1:p.Ile426Phe
|
|
|
ENST00000371953.8:c.757A>T
MANE Select
|
ENSP00000361021.3:p.Ile253Phe
|
|
|
ENST00000371953.7:c.757A>T
|
ENSP00000361021.3:p.Ile253Phe
|
|
|
ENST00000472832.2:c.184A>T
|
ENSP00000483066.1:p.Ile62Phe
|
|
|
NM_000314.5:c.757A>T
|
NP_000305.3:p.Ile253Phe
|
|
|
NM_000314.6:c.757A>T
|
NP_000305.3:p.Ile253Phe
|
|
|
NM_001304717.2:c.1276A>T
|
NP_001291646.2:p.Ile426Phe
|
|
|
NM_001304718.1:c.166A>T
|
NP_001291647.1:p.Ile56Phe
|
|
|
XM_006717926.2:c.712A>T
|
XP_006717989.1:p.Ile238Phe
|
|
|
XM_011539981.1:c.757A>T
|
XP_011538283.1:p.Ile253Phe
|
|
|
XM_011539982.1:c.661A>T
|
XP_011538284.1:p.Ile221Phe
|
|
|
XR_945791.1:n.1327A>T
|
|
|
|
NM_000314.7:c.757A>T
|
NP_000305.3:p.Ile253Phe
|
|
|
NM_001304717.5:c.1276A>T
|
NP_001291646.4:p.Ile426Phe
|
|
|
NM_001304718.2:c.166A>T
|
NP_001291647.1:p.Ile56Phe
|
|
|
NM_000314.8:c.757A>T
MANE Select
|
NP_000305.3:p.Ile253Phe
|
|
