ENST00000403733.8:c.3369G>T
MANE Select
|
ENSP00000384222.3:p.Lys1123Asn
|
|
ENST00000403733.7:c.3369G>T
|
ENSP00000384222.3:p.Lys1123Asn
|
|
ENST00000427431.5:c.*2761G>T
|
ENSP00000393342.1:n.*2761G>T
|
|
ENST00000438543.5:c.*1165G>T
|
ENSP00000413521.1:n.*1165G>T
|
|
ENST00000448232.6:c.3441G>T
|
ENSP00000398577.2:p.Lys1147Asn
|
|
ENST00000504005.5:c.2415G>T
|
ENSP00000427569.1:p.Lys805Asn
|
|
ENST00000508747.1:c.753G>T
|
ENSP00000420835.1:p.Lys251Asn
|
|
ENST00000513834.5:c.3222G>T
|
ENSP00000425054.1:p.Lys1074Asn
|
|
NM_024949.5:c.3369G>T
|
NP_079225.5:p.Lys1123Asn
|
|
XM_011532269.1:c.3441G>T
|
XP_011530571.1:p.Lys1147Asn
|
|
XM_011532269.3:c.3441G>T
|
XP_011530571.1:p.Lys1147Asn
|
|
XM_024454225.1:c.3147G>T
|
XP_024309993.1:p.Lys1049Asn
|
|
NM_024949.6:c.3369G>T
MANE Select
|
NP_079225.5:p.Lys1123Asn
|
|