ENST00000382103.7:c.1017A>C
MANE Select
|
ENSP00000371535.2:p.Lys339Asn
|
|
ENST00000680581.1:c.1017A>C
|
ENSP00000506483.1:p.Lys339Asn
|
|
ENST00000680824.1:n.2233A>C
|
|
|
ENST00000681071.1:n.1309A>C
|
|
|
ENST00000681341.1:n.2158A>C
|
|
|
ENST00000681948.1:c.1272A>C
|
ENSP00000505991.1:p.Lys424Asn
|
|
ENST00000358971.7:c.*815A>C
|
ENSP00000351857.3:n.*815A>C
|
|
ENST00000382103.6:c.1017A>C
|
ENSP00000371535.2:p.Lys339Asn
|
|
ENST00000503150.1:c.299A>C
|
|
|
ENST00000505513.1:n.317A>C
|
|
|
ENST00000514585.5:c.*718A>C
|
ENSP00000421880.1:n.*718A>C
|
|
NM_016955.3:c.1017A>C
|
NP_058651.3:p.Lys339Asn
|
|
XM_005248168.2:c.780A>C
|
XP_005248225.1:p.Lys260Asn
|
|
XM_006713965.2:c.837A>C
|
XP_006714028.1:p.Lys279Asn
|
|
XM_011513846.1:c.1014A>C
|
XP_011512148.1:p.Lys338Asn
|
|
XM_011513847.1:c.984A>C
|
XP_011512149.1:p.Lys328Asn
|
|
XM_011513848.1:c.837A>C
|
XP_011512150.1:p.Lys279Asn
|
|
XM_011513846.2:c.1014A>C
|
XP_011512148.1:p.Lys338Asn
|
|
XM_011513847.2:c.984A>C
|
XP_011512149.1:p.Lys328Asn
|
|
XM_017008277.1:c.1272A>C
|
XP_016863766.1:p.Lys424Asn
|
|
XM_017008278.1:c.594A>C
|
XP_016863767.1:p.Lys198Asn
|
|
NM_016955.4:c.1017A>C
MANE Select
|
NP_058651.3:p.Lys339Asn
|
|