ENST00000681978.1:n.2670C>G
|
|
|
ENST00000682178.1:n.2166C>G
|
|
|
ENST00000682345.1:c.*834C>G
|
ENSP00000508122.1:n.*834C>G
|
|
ENST00000682452.1:n.1465C>G
|
|
|
ENST00000682456.1:c.993C>G
|
ENSP00000508240.1:p.Thr331=
|
|
ENST00000682566.1:n.1917C>G
|
|
|
ENST00000682613.1:n.1446C>G
|
|
|
ENST00000682734.1:c.-40C>G
|
ENSP00000507860.1:n.-40C>G
|
|
ENST00000682820.1:n.1171C>G
|
|
|
ENST00000683004.1:c.*827C>G
|
ENSP00000506936.1:n.*827C>G
|
|
ENST00000683079.1:c.*559C>G
|
ENSP00000507296.1:n.*559C>G
|
|
ENST00000683081.1:c.*971C>G
|
ENSP00000507722.1:n.*971C>G
|
|
ENST00000683181.1:n.413C>G
|
|
|
ENST00000683209.1:n.3460C>G
|
|
|
ENST00000683305.1:c.951C>G
|
ENSP00000508043.1:p.Thr317=
|
|
ENST00000683448.1:c.*54C>G
|
ENSP00000506931.1:n.*54C>G
|
|
ENST00000683478.1:c.*485C>G
|
ENSP00000507793.1:n.*485C>G
|
|
ENST00000683483.1:c.990C>G
|
ENSP00000507719.1:p.Thr330=
|
|
ENST00000683622.1:n.848C>G
|
|
|
ENST00000683751.1:c.639C>G
|
ENSP00000506944.1:p.Thr213=
|
|
ENST00000684036.1:c.951C>G
|
ENSP00000507276.1:p.Thr317=
|
|
ENST00000684129.1:c.-40C>G
|
ENSP00000507174.1:n.-40C>G
|
|
ENST00000684209.1:n.1509C>G
|
|
|
ENST00000684296.1:c.*54C>G
|
ENSP00000507740.1:n.*54C>G
|
|
ENST00000684505.1:c.1083C>G
|
ENSP00000508237.1:p.Thr361=
|
|
ENST00000684552.1:c.*54C>G
|
ENSP00000506899.1:n.*54C>G
|
|
ENST00000684611.1:n.2862C>G
|
|
|
ENST00000684622.1:c.1134C>G
|
ENSP00000507546.1:p.Thr378=
|
|
ENST00000684627.1:c.951C>G
|
ENSP00000507471.1:p.Thr317=
|
|
ENST00000684641.1:c.849C>G
|
ENSP00000507642.1:p.Thr283=
|
|
ENST00000684675.1:c.1175C>G
|
ENSP00000506934.1:p.Pro392Arg
|
|
ENST00000684749.1:n.1203C>G
|
|
|
ENST00000511912.6:c.1134C>G
MANE Select
|
ENSP00000426638.1:p.Thr378=
|
|
ENST00000307738.5:c.993C>G
|
ENSP00000303552.5:p.Thr331=
|
|
ENST00000506422.1:n.104C>G
|
|
|
ENST00000511912.5:c.1134C>G
|
ENSP00000426638.1:p.Thr378=
|
|
NM_001281737.1:c.993C>G
|
NP_001268666.1:p.Thr331=
|
|
NM_001281738.1:c.951C>G
|
NP_001268667.1:p.Thr317=
|
|
NM_004453.3:c.1134C>G
|
NP_004444.2:p.Thr378=
|
|
XM_024453935.1:c.951C>G
|
XP_024309703.1:p.Thr317=
|
|
NM_004453.4:c.1134C>G
MANE Select
|
NP_004444.2:p.Thr378=
|
|
NM_001281737.2:c.993C>G
|
NP_001268666.1:p.Thr331=
|
|