ENST00000695850.1:n.1406T>G
|
|
|
ENST00000695852.1:n.337T>G
|
|
|
ENST00000695853.1:c.*1289T>G
|
ENSP00000512218.1:n.*1289T>G
|
|
ENST00000423902.7:c.8230T>G
MANE Select
|
ENSP00000392028.1:p.Leu2744Val
|
|
ENST00000423902.6:c.8230T>G
|
ENSP00000392028.1:p.Leu2744Val
|
|
ENST00000524602.5:c.2083T>G
|
ENSP00000437061.1:p.Leu695Val
|
|
ENST00000528280.1:n.276T>G
|
|
|
NM_001316690.1:c.2083T>G
|
NP_001303619.1:p.Leu695Val
|
|
NM_017780.3:c.8230T>G
|
NP_060250.2:p.Leu2744Val
|
|
XM_011517553.1:c.8320T>G
|
XP_011515855.1:p.Leu2774Val
|
|
XM_011517554.1:c.8320T>G
|
XP_011515856.1:p.Leu2774Val
|
|
XM_011517555.1:c.8317T>G
|
XP_011515857.1:p.Leu2773Val
|
|
XM_011517556.1:c.8098T>G
|
XP_011515858.1:p.Leu2700Val
|
|
XM_011517557.1:c.6307T>G
|
XP_011515859.1:p.Leu2103Val
|
|
XM_011517558.1:c.5857T>G
|
XP_011515860.1:p.Leu1953Val
|
|
XM_011517559.1:c.5065T>G
|
XP_011515861.1:p.Leu1689Val
|
|
XM_011517553.2:c.8320T>G
|
XP_011515855.1:p.Leu2774Val
|
|
XM_011517554.3:c.8320T>G
|
XP_011515856.1:p.Leu2774Val
|
|
XM_011517555.2:c.8317T>G
|
XP_011515857.1:p.Leu2773Val
|
|
XM_017013612.1:c.8320T>G
|
XP_016869101.1:p.Leu2774Val
|
|
XM_017013613.1:c.8227T>G
|
XP_016869102.1:p.Leu2743Val
|
|
NM_017780.4:c.8230T>G
MANE Select
|
NP_060250.2:p.Leu2744Val
|
|