ENST00000695850.1:n.1347A>T
|
|
|
ENST00000695852.1:n.278A>T
|
|
|
ENST00000695853.1:c.*1230A>T
|
ENSP00000512218.1:n.*1230A>T
|
|
ENST00000423902.7:c.8171A>T
MANE Select
|
ENSP00000392028.1:p.Glu2724Val
|
|
ENST00000423902.6:c.8171A>T
|
ENSP00000392028.1:p.Glu2724Val
|
|
ENST00000524602.5:c.2024A>T
|
ENSP00000437061.1:p.Glu675Val
|
|
ENST00000528280.1:n.217A>T
|
|
|
ENST00000532149.1:n.593A>T
|
|
|
ENST00000618450.1:n.4207A>T
|
|
|
NM_001316690.1:c.2024A>T
|
NP_001303619.1:p.Glu675Val
|
|
NM_017780.3:c.8171A>T
|
NP_060250.2:p.Glu2724Val
|
|
XM_011517553.1:c.8261A>T
|
XP_011515855.1:p.Glu2754Val
|
|
XM_011517554.1:c.8261A>T
|
XP_011515856.1:p.Glu2754Val
|
|
XM_011517555.1:c.8258A>T
|
XP_011515857.1:p.Glu2753Val
|
|
XM_011517556.1:c.8039A>T
|
XP_011515858.1:p.Glu2680Val
|
|
XM_011517557.1:c.6248A>T
|
XP_011515859.1:p.Glu2083Val
|
|
XM_011517558.1:c.5798A>T
|
XP_011515860.1:p.Glu1933Val
|
|
XM_011517559.1:c.5006A>T
|
XP_011515861.1:p.Glu1669Val
|
|
XM_011517553.2:c.8261A>T
|
XP_011515855.1:p.Glu2754Val
|
|
XM_011517554.3:c.8261A>T
|
XP_011515856.1:p.Glu2754Val
|
|
XM_011517555.2:c.8258A>T
|
XP_011515857.1:p.Glu2753Val
|
|
XM_017013612.1:c.8261A>T
|
XP_016869101.1:p.Glu2754Val
|
|
XM_017013613.1:c.8168A>T
|
XP_016869102.1:p.Glu2723Val
|
|
NM_017780.4:c.8171A>T
MANE Select
|
NP_060250.2:p.Glu2724Val
|
|