ENST00000255078.8:c.2528G>A
MANE Select
|
ENSP00000255078.4:p.Ser843Asn
|
|
ENST00000674675.1:c.673G>A
|
|
|
ENST00000674878.1:c.633G>A
|
|
|
ENST00000675118.1:c.2016G>A
|
|
|
ENST00000675389.1:n.803G>A
|
|
|
ENST00000675615.1:c.2528G>A
|
ENSP00000502413.1:p.Ser843Asn
|
|
ENST00000675648.1:n.1903G>A
|
|
|
ENST00000675916.1:c.772G>A
|
|
|
ENST00000676173.1:n.3273G>A
|
|
|
ENST00000676182.1:c.959G>A
|
|
|
ENST00000676228.1:c.*1851G>A
|
ENSP00000502375.1:n.*1851G>A
|
|
ENST00000255078.7:c.2528G>A
|
ENSP00000255078.3:p.Ser843Asn
|
|
ENST00000539064.5:n.2287G>A
|
|
|
ENST00000543739.5:n.1521G>A
|
|
|
NM_002180.2:c.2528G>A , LRG_250t1:c.2528G>A
|
NP_002171.2:p.Ser843Asn
|
|
XM_005273974.2:c.1517G>A
|
XP_005274031.1:p.Ser506Asn
|
|
XM_005273975.2:c.1400G>A
|
XP_005274032.1:p.Ser467Asn
|
|
XM_011544994.1:c.1295G>A
|
XP_011543296.1:p.Ser432Asn
|
|
XR_949903.1:n.2630G>A
|
|
|
XM_005273975.3:c.1400G>A
|
XP_005274032.1:p.Ser467Asn
|
|
XM_017017669.2:c.1517G>A
|
XP_016873158.1:p.Ser506Asn
|
|
XM_017017670.2:c.1517G>A
|
XP_016873159.1:p.Ser506Asn
|
|
XR_949903.3:n.2626G>A
|
|
|
NM_002180.3:c.2528G>A
MANE Select
|
NP_002171.2:p.Ser843Asn
|
|