ENST00000261769.10:c.1766A>C
MANE Select
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ENSP00000261769.4:p.Asn589Thr
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ENST00000261769.9:c.1766A>C
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ENSP00000261769.4:p.Asn589Thr
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ENST00000422392.6:c.1583A>C
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ENSP00000414946.2:p.Asn528Thr
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ENST00000562836.5:n.1837A>C
|
|
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ENST00000566510.5:c.*432A>C
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ENSP00000458139.1:n.*432A>C
|
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ENST00000566612.5:c.*6A>C
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ENSP00000454782.1:n.*6A>C
|
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ENST00000611625.4:c.1829A>C
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ENSP00000481063.1:p.Asn610Thr
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ENST00000612417.4:c.1766A>C
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ENSP00000478360.1:p.Asn589Thr
|
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ENST00000621016.4:c.1766A>C
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ENSP00000480664.1:p.Asn589Thr
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NM_004360.3:c.1766A>C , LRG_301t1:c.1766A>C
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NP_004351.1:p.Asn589Thr
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XM_011523488.1:c.1031A>C
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XP_011521790.1:p.Asn344Thr
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XM_011523489.1:c.1031A>C
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XP_011521791.1:p.Asn344Thr
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NM_001317184.1:c.1583A>C
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NP_001304113.1:p.Asn528Thr
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|
NM_001317185.1:c.218A>C
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NP_001304114.1:p.Asn73Thr
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|
NM_001317186.1:c.-200A>C
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NP_001304115.1:n.-200A>C
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|
NM_004360.4:c.1766A>C
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NP_004351.1:p.Asn589Thr
|
|
NM_004360.5:c.1766A>C
MANE Select
|
NP_004351.1:p.Asn589Thr
|
|
NM_001317184.2:c.1583A>C
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NP_001304113.1:p.Asn528Thr
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|
NM_001317185.2:c.218A>C
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NP_001304114.1:p.Asn73Thr
|
|
NM_001317186.2:c.-200A>C
|
NP_001304115.1:n.-200A>C
|
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