ENST00000367466.4:c.1366T>A
MANE Select
|
ENSP00000356436.3:p.Tyr456Asn
|
|
ENST00000367466.3:c.1366T>A
|
ENSP00000356436.3:p.Tyr456Asn
|
|
NM_001311193.1:c.1186T>A
|
NP_001298122.1:p.Tyr396Asn
|
|
NM_024420.2:c.1366T>A
|
NP_077734.1:p.Tyr456Asn
|
|
XM_005245267.2:c.1255T>A
|
XP_005245324.1:p.Tyr419Asn
|
|
XM_011509641.1:c.1387T>A
|
XP_011507943.1:p.Tyr463Asn
|
|
XM_011509642.1:c.1366T>A
|
XP_011507944.1:p.Tyr456Asn
|
|
XM_011509643.1:c.1366T>A
|
XP_011507945.1:p.Tyr456Asn
|
|
XR_921838.1:n.1427T>A
|
|
|
XM_005245267.4:c.1381T>A
|
XP_005245324.2:p.Tyr461Asn
|
|
XM_011509642.2:c.1366T>A
|
XP_011507944.1:p.Tyr456Asn
|
|
NM_001311193.2:c.1186T>A
|
NP_001298122.2:p.Tyr396Asn
|
|
NM_024420.3:c.1366T>A
MANE Select
|
NP_077734.2:p.Tyr456Asn
|
|