ENST00000264595.7:c.532T>A
MANE Select
|
ENSP00000264595.2:p.Tyr178Asn
|
|
ENST00000264595.6:c.532T>A
|
ENSP00000264595.2:p.Tyr178Asn
|
|
ENST00000502310.5:c.187T>A
|
ENSP00000423798.1:p.Tyr63Asn
|
|
ENST00000506853.5:n.566T>A
|
|
|
ENST00000510635.1:c.228T>A
|
|
|
ENST00000510955.5:n.453T>A
|
|
|
NM_000027.3:c.532T>A
|
NP_000018.2:p.Tyr178Asn
|
|
NM_001171988.1:c.532T>A
|
NP_001165459.1:p.Tyr178Asn
|
|
NR_033655.1:n.660T>A
|
|
|
XM_006714123.2:c.532T>A
|
XP_006714186.1:p.Tyr178Asn
|
|
XR_001741155.2:n.626T>A
|
|
|
NM_000027.4:c.532T>A
MANE Select
|
NP_000018.2:p.Tyr178Asn
|
|
NM_001171988.2:c.532T>A
|
NP_001165459.1:p.Tyr178Asn
|
|
NR_033655.2:n.594T>A
|
|
|