ENST00000261769.10:c.2469A>C
MANE Select
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ENSP00000261769.4:p.Thr823=
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ENST00000261769.9:c.2469A>C
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ENSP00000261769.4:p.Thr823=
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ENST00000422392.6:c.2286A>C
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ENSP00000414946.2:p.Thr762=
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ENST00000562118.1:n.687A>C
|
|
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ENST00000562836.5:n.2540A>C
|
|
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ENST00000566510.5:c.*1135A>C
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ENSP00000458139.1:n.*1135A>C
|
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ENST00000566612.5:c.*709A>C
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ENSP00000454782.1:n.*709A>C
|
|
ENST00000611625.4:c.2532A>C
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ENSP00000481063.1:p.Thr844=
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ENST00000612417.4:c.1854-872A>C
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ENSP00000478360.1:n.1854-872A>C
|
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ENST00000621016.4:c.1866-884A>C
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ENSP00000480664.1:n.1866-884A>C
|
|
NM_004360.3:c.2469A>C , LRG_301t1:c.2469A>C
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NP_004351.1:p.Thr823=
|
|
XM_011523488.1:c.1734A>C
|
XP_011521790.1:p.Thr578=
|
|
XM_011523489.1:c.1734A>C
|
XP_011521791.1:p.Thr578=
|
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NM_001317184.1:c.2286A>C
|
NP_001304113.1:p.Thr762=
|
|
NM_001317185.1:c.921A>C
|
NP_001304114.1:p.Thr307=
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|
NM_001317186.1:c.504A>C
|
NP_001304115.1:p.Thr168=
|
|
NM_004360.4:c.2469A>C
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NP_004351.1:p.Thr823=
|
|
NM_004360.5:c.2469A>C
MANE Select
|
NP_004351.1:p.Thr823=
|
|
NM_001317184.2:c.2286A>C
|
NP_001304113.1:p.Thr762=
|
|
NM_001317185.2:c.921A>C
|
NP_001304114.1:p.Thr307=
|
|
NM_001317186.2:c.504A>C
|
NP_001304115.1:p.Thr168=
|
|