ENST00000642524.1:c.*1806T>G
|
ENSP00000493766.1:n.*1806T>G
|
|
ENST00000643051.1:c.1773T>G
|
ENSP00000495513.1:p.Thr591=
|
|
ENST00000643556.1:c.1914T>G
|
ENSP00000494938.1:n.1914T>G
|
|
ENST00000643816.1:n.2056T>G
|
|
|
ENST00000643842.1:c.*1819T>G
|
ENSP00000493861.1:n.*1819T>G
|
|
ENST00000644471.1:n.1864T>G
|
|
|
ENST00000645237.2:c.1773T>G
MANE Select
|
ENSP00000494609.1:p.Thr591=
|
|
ENST00000645532.1:c.1812T>G
|
ENSP00000494431.1:p.Thr604=
|
|
ENST00000646439.1:c.1773T>G
|
ENSP00000494751.1:p.Thr591=
|
|
ENST00000376887.8:c.1773T>G
|
ENSP00000366084.4:p.Thr591=
|
|
ENST00000536256.3:c.1548T>G
|
ENSP00000442024.1:p.Thr516=
|
|
ENST00000629385.1:c.1773T>G
|
ENSP00000487081.1:p.Thr591=
|
|
NM_001105515.2:c.1773T>G
|
NP_001098985.1:p.Thr591=
|
|
NM_001301829.1:c.1773T>G
|
NP_001288758.1:p.Thr591=
|
|
NM_001301830.1:c.1548T>G
|
NP_001288759.1:p.Thr516=
|
|
NM_005845.4:c.1773T>G
|
NP_005836.2:p.Thr591=
|
|
XM_005254025.2:c.1644T>G
|
XP_005254082.1:p.Thr548=
|
|
XM_006719914.1:c.1683T>G
|
XP_006719977.1:p.Thr561=
|
|
XM_011521047.1:c.1224T>G
|
XP_011519349.1:p.Thr408=
|
|
XM_017020319.1:c.1644T>G
|
XP_016875808.1:p.Thr548=
|
|
XM_017020320.2:c.1773T>G
|
XP_016875809.1:p.Thr591=
|
|
XM_017020321.1:c.258T>G
|
XP_016875810.1:p.Thr86=
|
|
XM_017020322.1:c.1644T>G
|
XP_016875811.1:p.Thr548=
|
|
NM_001105515.3:c.1773T>G
|
NP_001098985.1:p.Thr591=
|
|
NM_001301829.2:c.1773T>G
|
NP_001288758.1:p.Thr591=
|
|
NM_001301830.2:c.1548T>G
|
NP_001288759.1:p.Thr516=
|
|
NM_005845.5:c.1773T>G
MANE Select
|
NP_005836.2:p.Thr591=
|
|