ENST00000261769.10:c.2004G>C
MANE Select
|
ENSP00000261769.4:p.Lys668Asn
|
|
ENST00000261769.9:c.2004G>C
|
ENSP00000261769.4:p.Lys668Asn
|
|
ENST00000422392.6:c.1821G>C
|
ENSP00000414946.2:p.Lys607Asn
|
|
ENST00000562118.1:n.222G>C
|
|
|
ENST00000562836.5:n.2075G>C
|
|
|
ENST00000566510.5:c.*670G>C
|
ENSP00000458139.1:n.*670G>C
|
|
ENST00000566612.5:c.*244G>C
|
ENSP00000454782.1:n.*244G>C
|
|
ENST00000611625.4:c.2067G>C
|
ENSP00000481063.1:p.Lys689Asn
|
|
ENST00000612417.4:c.1830+1347G>C
|
ENSP00000478360.1:n.1830+1347G>C
|
|
ENST00000621016.4:c.1865+1312G>C
|
ENSP00000480664.1:n.1865+1312G>C
|
|
NM_004360.3:c.2004G>C , LRG_301t1:c.2004G>C
|
NP_004351.1:p.Lys668Asn
|
|
XM_011523488.1:c.1269G>C
|
XP_011521790.1:p.Lys423Asn
|
|
XM_011523489.1:c.1269G>C
|
XP_011521791.1:p.Lys423Asn
|
|
NM_001317184.1:c.1821G>C
|
NP_001304113.1:p.Lys607Asn
|
|
NM_001317185.1:c.456G>C
|
NP_001304114.1:p.Lys152Asn
|
|
NM_001317186.1:c.39G>C
|
NP_001304115.1:p.Lys13Asn
|
|
NM_004360.4:c.2004G>C
|
NP_004351.1:p.Lys668Asn
|
|
NM_004360.5:c.2004G>C
MANE Select
|
NP_004351.1:p.Lys668Asn
|
|
NM_001317184.2:c.1821G>C
|
NP_001304113.1:p.Lys607Asn
|
|
NM_001317185.2:c.456G>C
|
NP_001304114.1:p.Lys152Asn
|
|
NM_001317186.2:c.39G>C
|
NP_001304115.1:p.Lys13Asn
|
|