ENST00000261769.10:c.753G=
MANE Select
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ENSP00000261769.4:p.Thr251=
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ENST00000261769.9:c.753G=
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ENSP00000261769.4:p.Thr251=
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|
ENST00000422392.6:c.753G=
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ENSP00000414946.2:p.Thr251=
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ENST00000561751.1:c.454+1414G=
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|
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ENST00000562836.5:n.824G=
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|
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ENST00000566510.5:c.597G=
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ENSP00000458139.1:p.Thr199=
|
|
ENST00000566612.5:c.753G=
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ENSP00000454782.1:p.Thr251=
|
|
ENST00000611625.4:c.753G=
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ENSP00000481063.1:p.Thr251=
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ENST00000612417.4:c.753G=
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ENSP00000478360.1:p.Thr251=
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|
ENST00000621016.4:c.753G=
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ENSP00000480664.1:p.Thr251=
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|
NM_004360.3:c.753G= , LRG_301t1:c.753G=
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NP_004351.1:p.Thr251=
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|
XM_011523488.1:c.18G=
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XP_011521790.1:p.Thr6=
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|
XM_011523489.1:c.18G=
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XP_011521791.1:p.Thr6=
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|
NM_001317184.1:c.753G=
|
NP_001304113.1:p.Thr251=
|
|
NM_001317185.1:c.-863G=
|
NP_001304114.1:n.-863G=
|
|
NM_001317186.1:c.-1067G=
|
NP_001304115.1:n.-1067G=
|
|
NM_004360.4:c.753G=
|
NP_004351.1:p.Thr251=
|
|
NM_004360.5:c.753G=
MANE Select
|
NP_004351.1:p.Thr251=
|
|
NM_001317184.2:c.753G=
|
NP_001304113.1:p.Thr251=
|
|
NM_001317185.2:c.-863G=
|
NP_001304114.1:n.-863G=
|
|
NM_001317186.2:c.-1067G=
|
NP_001304115.1:n.-1067G=
|
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