ENST00000342245.9:c.1555T>A
MANE Select
|
ENSP00000340409.4:p.Tyr519Asn
|
|
ENST00000342245.8:c.1555T>A
|
ENSP00000340409.4:p.Tyr519Asn
|
|
ENST00000526280.1:c.612T>A
|
|
|
ENST00000527275.5:c.1552T>A
|
ENSP00000435350.1:p.Tyr518Asn
|
|
ENST00000531303.5:c.*406T>A
|
ENSP00000432625.1:n.*406T>A
|
|
ENST00000531336.1:n.543T>A
|
|
|
ENST00000533123.5:c.*282T>A
|
ENSP00000435950.1:n.*282T>A
|
|
ENST00000534405.5:c.*386T>A
|
ENSP00000434353.1:n.*386T>A
|
|
NM_000543.4:c.1555T>A
|
NP_000534.3:p.Tyr519Asn
|
|
NM_001007593.2:c.1552T>A
|
NP_001007594.2:p.Tyr518Asn
|
|
XM_005253075.3:c.*48T>A
|
XP_005253132.1:n.*48T>A
|
|
XM_011520303.1:c.1423T>A
|
XP_011518605.1:p.Tyr475Asn
|
|
XM_011520304.1:c.*48T>A
|
XP_011518606.1:n.*48T>A
|
|
NM_001318087.1:c.*48T>A
|
NP_001305016.1:n.*48T>A
|
|
NM_001318088.1:c.634T>A
|
NP_001305017.1:p.Tyr212Asn
|
|
NM_001365135.1:c.1423T>A
|
NP_001352064.1:p.Tyr475Asn
|
|
NR_027400.2:n.1568T>A
|
|
|
NR_134502.1:n.1107T>A
|
|
|
XM_011520304.2:c.*48T>A
|
XP_011518606.1:n.*48T>A
|
|
XR_001747940.2:n.1740T>A
|
|
|
XR_002957158.1:n.1922T>A
|
|
|
NM_000543.5:c.1555T>A
MANE Select
|
NP_000534.3:p.Tyr519Asn
|
|
NM_001007593.3:c.1552T>A
|
NP_001007594.2:p.Tyr518Asn
|
|
NM_001318087.2:c.*48T>A
|
NP_001305016.1:n.*48T>A
|
|
NM_001318088.2:c.634T>A
|
NP_001305017.1:p.Tyr212Asn
|
|
NM_001365135.2:c.1423T>A
|
NP_001352064.1:p.Tyr475Asn
|
|
NR_027400.3:n.1508T>A
|
|
|
NR_134502.2:n.1047T>A
|
|
|