ENST00000697149.1:c.1726G>T
|
ENSP00000513138.1:n.1726G>T
|
|
ENST00000697150.1:c.1784G>T
|
ENSP00000513139.1:n.1784G>T
|
|
ENST00000697151.1:c.1717G>T
|
ENSP00000513140.1:n.1717G>T
|
|
ENST00000697164.1:c.1797G>T
|
ENSP00000513153.1:p.Lys599Asn
|
|
ENST00000697165.1:c.1584G>T
|
ENSP00000513154.1:p.Lys528Asn
|
|
ENST00000347310.10:c.1887G>T
MANE Select
|
ENSP00000321345.5:p.Lys629Asn
|
|
ENST00000637002.1:c.1278G>T
|
ENSP00000490340.1:p.Lys426Asn
|
|
ENST00000347310.9:c.1887G>T
|
ENSP00000321345.5:p.Lys629Asn
|
|
ENST00000395227.2:c.681G>T
|
ENSP00000378652.2:p.Lys227Asn
|
|
ENST00000425614.3:c.1122G>T
|
ENSP00000387640.2:p.Lys374Asn
|
|
ENST00000473881.2:c.*713G>T
|
ENSP00000486667.1:n.*713G>T
|
|
NM_144701.2:c.1887G>T
|
NP_653302.2:p.Lys629Asn
|
|
XM_005270516.2:c.1125G>T
|
XP_005270573.1:p.Lys375Asn
|
|
XM_011540789.1:c.1977G>T
|
XP_011539091.1:p.Lys659Asn
|
|
XM_011540790.1:c.1887G>T
|
XP_011539092.1:p.Lys629Asn
|
|
XM_011540791.1:c.1887G>T
|
XP_011539093.1:p.Lys629Asn
|
|
XM_011540790.3:c.1887G>T
|
XP_011539092.1:p.Lys629Asn
|
|
XM_011540791.3:c.1887G>T
|
XP_011539093.1:p.Lys629Asn
|
|
XR_001736993.1:n.1967G>T
|
|
|
NM_144701.3:c.1887G>T
MANE Select
|
NP_653302.2:p.Lys629Asn
|
|