ENST00000261769.10:c.1797T>G
MANE Select
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ENSP00000261769.4:p.Thr599=
|
|
ENST00000261769.9:c.1797T>G
|
ENSP00000261769.4:p.Thr599=
|
|
ENST00000422392.6:c.1614T>G
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ENSP00000414946.2:p.Thr538=
|
|
ENST00000562836.5:n.1868T>G
|
|
|
ENST00000566510.5:c.*463T>G
|
ENSP00000458139.1:n.*463T>G
|
|
ENST00000566612.5:c.*37T>G
|
ENSP00000454782.1:n.*37T>G
|
|
ENST00000611625.4:c.1860T>G
|
ENSP00000481063.1:p.Thr620=
|
|
ENST00000612417.4:c.1797T>G
|
ENSP00000478360.1:p.Thr599=
|
|
ENST00000621016.4:c.1797T>G
|
ENSP00000480664.1:p.Thr599=
|
|
NM_004360.3:c.1797T>G , LRG_301t1:c.1797T>G
|
NP_004351.1:p.Thr599=
|
|
XM_011523488.1:c.1062T>G
|
XP_011521790.1:p.Thr354=
|
|
XM_011523489.1:c.1062T>G
|
XP_011521791.1:p.Thr354=
|
|
NM_001317184.1:c.1614T>G
|
NP_001304113.1:p.Thr538=
|
|
NM_001317185.1:c.249T>G
|
NP_001304114.1:p.Thr83=
|
|
NM_001317186.1:c.-169T>G
|
NP_001304115.1:n.-169T>G
|
|
NM_004360.4:c.1797T>G
|
NP_004351.1:p.Thr599=
|
|
NM_004360.5:c.1797T>G
MANE Select
|
NP_004351.1:p.Thr599=
|
|
NM_001317184.2:c.1614T>G
|
NP_001304113.1:p.Thr538=
|
|
NM_001317185.2:c.249T>G
|
NP_001304114.1:p.Thr83=
|
|
NM_001317186.2:c.-169T>G
|
NP_001304115.1:n.-169T>G
|
|