ENST00000358691.10:c.3270G>T
MANE Select
|
ENSP00000351524.5:p.Glu1090Asp
|
|
ENST00000358691.9:c.3270G>T
|
ENSP00000351524.5:p.Glu1090Asp
|
|
ENST00000579953.5:c.3273G>T
|
ENSP00000463727.1:p.Glu1091Asp
|
|
ENST00000580168.5:c.3273G>T
|
ENSP00000464512.1:p.Glu1091Asp
|
|
NM_014877.3:c.3270G>T
|
NP_055692.2:p.Glu1090Asp
|
|
XM_005257888.3:c.3351G>T
|
XP_005257945.1:p.Glu1117Asp
|
|
XM_005257889.3:c.3273G>T
|
XP_005257946.1:p.Glu1091Asp
|
|
XM_005257890.3:c.3249G>T
|
XP_005257947.1:p.Glu1083Asp
|
|
XM_006722214.2:c.3354G>T
|
XP_006722277.1:p.Glu1118Asp
|
|
XM_006722215.2:c.2649G>T
|
XP_006722278.1:p.Glu883Asp
|
|
XM_006722216.2:c.2178G>T
|
XP_006722279.1:p.Glu726Asp
|
|
XM_011525544.1:c.3354G>T
|
XP_011523846.1:p.Glu1118Asp
|
|
XM_011525545.1:c.3354G>T
|
XP_011523847.1:p.Glu1118Asp
|
|
XR_934629.1:n.3345G>T
|
|
|
NM_001330447.1:c.3273G>T
|
NP_001317376.1:p.Glu1091Asp
|
|
XM_005257888.5:c.3351G>T
|
XP_005257945.1:p.Glu1117Asp
|
|
XM_006722214.4:c.3354G>T
|
XP_006722277.1:p.Glu1118Asp
|
|
XM_006722215.3:c.2649G>T
|
XP_006722278.1:p.Glu883Asp
|
|
XM_006722216.3:c.2178G>T
|
XP_006722279.1:p.Glu726Asp
|
|
XM_011525544.2:c.3354G>T
|
XP_011523846.1:p.Glu1118Asp
|
|
XM_017025477.2:c.2565G>T
|
XP_016880966.1:p.Glu855Asp
|
|
XM_017025478.1:c.2097G>T
|
XP_016880967.1:p.Glu699Asp
|
|
XR_001752712.2:n.3445G>T
|
|
|
XR_001752713.2:n.3297G>T
|
|
|
XR_001752714.2:n.3213G>T
|
|
|
NM_014877.4:c.3270G>T
MANE Select
|
NP_055692.3:p.Glu1090Asp
|
|
NM_001330447.2:c.3273G>T
|
NP_001317376.2:p.Glu1091Asp
|
|