ENST00000681978.1:n.2675C>G
|
|
|
ENST00000682178.1:n.2171C>G
|
|
|
ENST00000682345.1:c.*839C>G
|
ENSP00000508122.1:n.*839C>G
|
|
ENST00000682452.1:n.1470C>G
|
|
|
ENST00000682456.1:c.998C>G
|
ENSP00000508240.1:p.Pro333Arg
|
|
ENST00000682566.1:n.1922C>G
|
|
|
ENST00000682613.1:n.1451C>G
|
|
|
ENST00000682734.1:c.-35C>G
|
ENSP00000507860.1:n.-35C>G
|
|
ENST00000682820.1:n.1176C>G
|
|
|
ENST00000683004.1:c.*832C>G
|
ENSP00000506936.1:n.*832C>G
|
|
ENST00000683079.1:c.*564C>G
|
ENSP00000507296.1:n.*564C>G
|
|
ENST00000683081.1:c.*976C>G
|
ENSP00000507722.1:n.*976C>G
|
|
ENST00000683181.1:n.418C>G
|
|
|
ENST00000683209.1:n.3465C>G
|
|
|
ENST00000683305.1:c.956C>G
|
ENSP00000508043.1:p.Pro319Arg
|
|
ENST00000683448.1:c.*59C>G
|
ENSP00000506931.1:n.*59C>G
|
|
ENST00000683478.1:c.*490C>G
|
ENSP00000507793.1:n.*490C>G
|
|
ENST00000683483.1:c.995C>G
|
ENSP00000507719.1:p.Pro332Arg
|
|
ENST00000683622.1:n.853C>G
|
|
|
ENST00000683751.1:c.644C>G
|
ENSP00000506944.1:p.Pro215Arg
|
|
ENST00000684036.1:c.956C>G
|
ENSP00000507276.1:p.Pro319Arg
|
|
ENST00000684129.1:c.-35C>G
|
ENSP00000507174.1:n.-35C>G
|
|
ENST00000684209.1:n.1514C>G
|
|
|
ENST00000684296.1:c.*59C>G
|
ENSP00000507740.1:n.*59C>G
|
|
ENST00000684505.1:c.1088C>G
|
ENSP00000508237.1:p.Pro363Arg
|
|
ENST00000684552.1:c.*59C>G
|
ENSP00000506899.1:n.*59C>G
|
|
ENST00000684611.1:n.2867C>G
|
|
|
ENST00000684622.1:c.1139C>G
|
ENSP00000507546.1:p.Pro380Arg
|
|
ENST00000684627.1:c.956C>G
|
ENSP00000507471.1:p.Pro319Arg
|
|
ENST00000684641.1:c.854C>G
|
ENSP00000507642.1:p.Pro285Arg
|
|
ENST00000684675.1:c.1180C>G
|
ENSP00000506934.1:p.Leu394Val
|
|
ENST00000684749.1:n.1208C>G
|
|
|
ENST00000511912.6:c.1139C>G
MANE Select
|
ENSP00000426638.1:p.Pro380Arg
|
|
ENST00000307738.5:c.998C>G
|
ENSP00000303552.5:p.Pro333Arg
|
|
ENST00000506422.1:n.109C>G
|
|
|
ENST00000511912.5:c.1139C>G
|
ENSP00000426638.1:p.Pro380Arg
|
|
NM_001281737.1:c.998C>G
|
NP_001268666.1:p.Pro333Arg
|
|
NM_001281738.1:c.956C>G
|
NP_001268667.1:p.Pro319Arg
|
|
NM_004453.3:c.1139C>G
|
NP_004444.2:p.Pro380Arg
|
|
XM_024453935.1:c.956C>G
|
XP_024309703.1:p.Pro319Arg
|
|
NM_004453.4:c.1139C>G
MANE Select
|
NP_004444.2:p.Pro380Arg
|
|
NM_001281737.2:c.998C>G
|
NP_001268666.1:p.Pro333Arg
|
|