ENST00000697149.1:c.1465C>A
|
ENSP00000513138.1:n.1465C>A
|
|
ENST00000697150.1:c.1523C>A
|
ENSP00000513139.1:n.1523C>A
|
|
ENST00000697151.1:c.1456C>A
|
ENSP00000513140.1:n.1456C>A
|
|
ENST00000697164.1:c.1536C>A
|
ENSP00000513153.1:p.Asn512Lys
|
|
ENST00000697165.1:c.1323C>A
|
ENSP00000513154.1:p.Asn441Lys
|
|
ENST00000347310.10:c.1626C>A
MANE Select
|
ENSP00000321345.5:p.Asn542Lys
|
|
ENST00000637002.1:c.1017C>A
|
ENSP00000490340.1:p.Asn339Lys
|
|
ENST00000347310.9:c.1626C>A
|
ENSP00000321345.5:p.Asn542Lys
|
|
ENST00000395227.2:c.420C>A
|
ENSP00000378652.2:p.Asn140Lys
|
|
ENST00000425614.3:c.861C>A
|
ENSP00000387640.2:p.Asn287Lys
|
|
ENST00000473881.2:c.*452C>A
|
ENSP00000486667.1:n.*452C>A
|
|
NM_144701.2:c.1626C>A
|
NP_653302.2:p.Asn542Lys
|
|
XM_005270516.2:c.864C>A
|
XP_005270573.1:p.Asn288Lys
|
|
XM_011540789.1:c.1716C>A
|
XP_011539091.1:p.Asn572Lys
|
|
XM_011540790.1:c.1626C>A
|
XP_011539092.1:p.Asn542Lys
|
|
XM_011540791.1:c.1626C>A
|
XP_011539093.1:p.Asn542Lys
|
|
XM_011540790.3:c.1626C>A
|
XP_011539092.1:p.Asn542Lys
|
|
XM_011540791.3:c.1626C>A
|
XP_011539093.1:p.Asn542Lys
|
|
XR_001736993.1:n.1706C>A
|
|
|
NM_144701.3:c.1626C>A
MANE Select
|
NP_653302.2:p.Asn542Lys
|
|