ENST00000261769.10:c.2545A>G
MANE Select
|
ENSP00000261769.4:p.Asn849Asp
|
|
ENST00000261769.9:c.2545A>G
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ENSP00000261769.4:p.Asn849Asp
|
|
ENST00000422392.6:c.2362A>G
|
ENSP00000414946.2:p.Asn788Asp
|
|
ENST00000562118.1:n.763A>G
|
|
|
ENST00000562836.5:n.2616A>G
|
|
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ENST00000566510.5:c.*1211A>G
|
ENSP00000458139.1:n.*1211A>G
|
|
ENST00000566612.5:c.*785A>G
|
ENSP00000454782.1:n.*785A>G
|
|
ENST00000611625.4:c.2608A>G
|
ENSP00000481063.1:p.Asn870Asp
|
|
ENST00000612417.4:c.1854-796A>G
|
ENSP00000478360.1:n.1854-796A>G
|
|
ENST00000621016.4:c.1866-808A>G
|
ENSP00000480664.1:n.1866-808A>G
|
|
NM_004360.3:c.2545A>G , LRG_301t1:c.2545A>G
|
NP_004351.1:p.Asn849Asp
|
|
XM_011523488.1:c.1810A>G
|
XP_011521790.1:p.Asn604Asp
|
|
XM_011523489.1:c.1810A>G
|
XP_011521791.1:p.Asn604Asp
|
|
NM_001317184.1:c.2362A>G
|
NP_001304113.1:p.Asn788Asp
|
|
NM_001317185.1:c.997A>G
|
NP_001304114.1:p.Asn333Asp
|
|
NM_001317186.1:c.580A>G
|
NP_001304115.1:p.Asn194Asp
|
|
NM_004360.4:c.2545A>G
|
NP_004351.1:p.Asn849Asp
|
|
NM_004360.5:c.2545A>G
MANE Select
|
NP_004351.1:p.Asn849Asp
|
|
NM_001317184.2:c.2362A>G
|
NP_001304113.1:p.Asn788Asp
|
|
NM_001317185.2:c.997A>G
|
NP_001304114.1:p.Asn333Asp
|
|
NM_001317186.2:c.580A>G
|
NP_001304115.1:p.Asn194Asp
|
|