ENST00000333868.10:c.448G>A
MANE Select
|
ENSP00000330237.5:p.Asp150Asn
|
|
ENST00000333868.9:c.448G>A
|
ENSP00000330237.5:p.Asp150Asn
|
|
ENST00000348549.9:c.418+10232G>A
|
ENSP00000255256.7:n.418+10232G>A
|
|
ENST00000375890.8:c.199G>A
|
ENSP00000365051.4:p.Asp67Asn
|
|
ENST00000400777.7:c.440G>A
|
|
|
ENST00000440484.1:c.448G>A
|
ENSP00000411304.1:p.Asp150Asn
|
|
ENST00000447522.5:c.199G>A
|
ENSP00000396540.1:p.Asp67Asn
|
|
ENST00000474305.2:c.308G>A
|
ENSP00000449216.1:n.308G>A
|
|
ENST00000546424.5:c.448G>A
|
ENSP00000449584.1:p.Asp150Asn
|
|
ENST00000546969.1:n.463G>A
|
|
|
NM_001229.4:c.448G>A
|
NP_001220.2:p.Asp150Asn
|
|
NM_001278054.1:c.418+10232G>A
|
NP_001264983.1:n.418+10232G>A
|
|
NM_032996.3:c.199G>A
|
NP_127463.2:p.Asp67Asn
|
|
NR_102732.1:n.693G>A
|
|
|
NR_102733.1:n.553G>A
|
|
|
XM_005246014.2:c.199G>A
|
XP_005246071.1:p.Asp67Asn
|
|
XM_011542270.1:c.448G>A
|
XP_011540572.1:p.Asp150Asn
|
|
XM_011542271.1:c.199G>A
|
XP_011540573.1:p.Asp67Asn
|
|
XM_011542272.1:c.199G>A
|
XP_011540574.1:p.Asp67Asn
|
|
XM_011542273.1:c.448G>A
|
XP_011540575.1:p.Asp150Asn
|
|
XR_946778.1:n.613G>A
|
|
|
XM_011542273.3:c.448G>A
|
XP_011540575.1:p.Asp150Asn
|
|
NM_001229.5:c.448G>A
MANE Select
|
NP_001220.2:p.Asp150Asn
|
|
NM_001278054.2:c.418+10232G>A
|
NP_001264983.1:n.418+10232G>A
|
|
NR_102732.2:n.463G>A
|
|
|
NR_102733.2:n.323G>A
|
|
|