ENST00000255078.8:c.2085G>T
MANE Select
|
ENSP00000255078.4:p.Lys695Asn
|
|
ENST00000674675.1:c.329G>T
|
|
|
ENST00000674878.1:c.329G>T
|
|
|
ENST00000674955.1:c.*802G>T
|
ENSP00000502463.1:n.*802G>T
|
|
ENST00000675118.1:c.1573G>T
|
|
|
ENST00000675389.1:n.360G>T
|
|
|
ENST00000675615.1:c.2085G>T
|
ENSP00000502413.1:p.Lys695Asn
|
|
ENST00000675648.1:n.1460G>T
|
|
|
ENST00000675916.1:c.329G>T
|
|
|
ENST00000676173.1:n.2830G>T
|
|
|
ENST00000676182.1:c.516G>T
|
|
|
ENST00000676228.1:c.*1408G>T
|
ENSP00000502375.1:n.*1408G>T
|
|
ENST00000255078.7:c.2085G>T
|
ENSP00000255078.3:p.Lys695Asn
|
|
ENST00000539064.5:n.1844G>T
|
|
|
ENST00000543739.5:n.1078G>T
|
|
|
NM_002180.2:c.2085G>T , LRG_250t1:c.2085G>T
|
NP_002171.2:p.Lys695Asn
|
|
XM_005273974.2:c.1074G>T
|
XP_005274031.1:p.Lys358Asn
|
|
XM_005273975.2:c.957G>T
|
XP_005274032.1:p.Lys319Asn
|
|
XM_011544994.1:c.852G>T
|
XP_011543296.1:p.Lys284Asn
|
|
XR_949903.1:n.2187G>T
|
|
|
XM_005273975.3:c.957G>T
|
XP_005274032.1:p.Lys319Asn
|
|
XM_017017669.2:c.1074G>T
|
XP_016873158.1:p.Lys358Asn
|
|
XM_017017670.2:c.1074G>T
|
XP_016873159.1:p.Lys358Asn
|
|
XR_949903.3:n.2183G>T
|
|
|
NM_002180.3:c.2085G>T
MANE Select
|
NP_002171.2:p.Lys695Asn
|
|