ENST00000700029.2:c.1066C>T
|
ENSP00000514759.2:p.Leu356Phe
|
|
ENST00000710265.1:c.973C>T
|
ENSP00000518161.1:p.Leu325Phe
|
|
ENST00000472832.3:c.973C>T
|
ENSP00000483066.2:p.Leu325Phe
|
|
ENST00000688158.2:n.1708C>T
|
|
|
ENST00000688922.2:c.*803C>T
|
ENSP00000508742.2:n.*803C>T
|
|
ENST00000700021.1:c.928C>T
|
ENSP00000514757.1:p.Leu310Phe
|
|
ENST00000700022.1:c.*312C>T
|
ENSP00000514758.1:n.*312C>T
|
|
ENST00000700023.1:n.2131C>T
|
|
|
ENST00000700024.1:n.2365C>T
|
|
|
ENST00000700025.1:n.1742C>T
|
|
|
ENST00000700026.1:n.610C>T
|
|
|
ENST00000706954.1:c.973C>T
|
ENSP00000516674.1:p.Leu325Phe
|
|
ENST00000706955.1:c.*1008C>T
|
ENSP00000516675.1:n.*1008C>T
|
|
ENST00000686459.1:c.*559C>T
|
ENSP00000508909.1:n.*559C>T
|
|
ENST00000688158.1:c.*1084C>T
|
ENSP00000509254.1:n.*1084C>T
|
|
ENST00000688308.1:c.973C>T
|
ENSP00000508752.1:p.Leu325Phe
|
|
ENST00000688922.1:c.894C>T
|
|
|
ENST00000693560.1:c.1492C>T
|
ENSP00000509861.1:p.Leu498Phe
|
|
ENST00000371953.8:c.973C>T
MANE Select
|
ENSP00000361021.3:p.Leu325Phe
|
|
ENST00000371953.7:c.973C>T
|
ENSP00000361021.3:p.Leu325Phe
|
|
ENST00000472832.2:c.400C>T
|
ENSP00000483066.1:p.Leu134Phe
|
|
NM_000314.5:c.973C>T
|
NP_000305.3:p.Leu325Phe
|
|
NM_000314.6:c.973C>T
|
NP_000305.3:p.Leu325Phe
|
|
NM_001304717.2:c.1492C>T
|
NP_001291646.2:p.Leu498Phe
|
|
NM_001304718.1:c.382C>T
|
NP_001291647.1:p.Leu128Phe
|
|
XM_006717926.2:c.928C>T
|
XP_006717989.1:p.Leu310Phe
|
|
XM_011539981.1:c.973C>T
|
XP_011538283.1:p.Leu325Phe
|
|
XM_011539982.1:c.877C>T
|
XP_011538284.1:p.Leu293Phe
|
|
XR_945791.1:n.1543C>T
|
|
|
NM_000314.7:c.973C>T
|
NP_000305.3:p.Leu325Phe
|
|
NM_001304717.5:c.1492C>T
|
NP_001291646.4:p.Leu498Phe
|
|
NM_001304718.2:c.382C>T
|
NP_001291647.1:p.Leu128Phe
|
|
NM_000314.8:c.973C>T
MANE Select
|
NP_000305.3:p.Leu325Phe
|
|