ENST00000695850.1:n.897T>A
|
|
|
ENST00000695851.1:n.101T>A
|
|
|
ENST00000695853.1:c.*780T>A
|
ENSP00000512218.1:n.*780T>A
|
|
ENST00000423902.7:c.7721T>A
MANE Select
|
ENSP00000392028.1:p.Leu2574His
|
|
ENST00000423902.6:c.7721T>A
|
ENSP00000392028.1:p.Leu2574His
|
|
ENST00000524602.5:c.1717-1213T>A
|
ENSP00000437061.1:n.1717-1213T>A
|
|
ENST00000531695.1:n.145T>A
|
|
|
ENST00000618450.1:n.113T>A
|
|
|
NM_001316690.1:c.1717-1213T>A
|
NP_001303619.1:n.1717-1213T>A
|
|
NM_017780.3:c.7721T>A
|
NP_060250.2:p.Leu2574His
|
|
XM_011517553.1:c.7811T>A
|
XP_011515855.1:p.Leu2604His
|
|
XM_011517554.1:c.7811T>A
|
XP_011515856.1:p.Leu2604His
|
|
XM_011517555.1:c.7808T>A
|
XP_011515857.1:p.Leu2603His
|
|
XM_011517556.1:c.7699-1180T>A
|
XP_011515858.1:n.7699-1180T>A
|
|
XM_011517557.1:c.5798T>A
|
XP_011515859.1:p.Leu1933His
|
|
XM_011517558.1:c.5348T>A
|
XP_011515860.1:p.Leu1783His
|
|
XM_011517559.1:c.4556T>A
|
XP_011515861.1:p.Leu1519His
|
|
XM_011517553.2:c.7811T>A
|
XP_011515855.1:p.Leu2604His
|
|
XM_011517554.3:c.7811T>A
|
XP_011515856.1:p.Leu2604His
|
|
XM_011517555.2:c.7808T>A
|
XP_011515857.1:p.Leu2603His
|
|
XM_017013612.1:c.7811T>A
|
XP_016869101.1:p.Leu2604His
|
|
XM_017013613.1:c.7718T>A
|
XP_016869102.1:p.Leu2573His
|
|
NM_017780.4:c.7721T>A
MANE Select
|
NP_060250.2:p.Leu2574His
|
|