ENST00000355773.6:c.1261T>A
MANE Select
|
ENSP00000348019.5:p.Tyr421Asn
|
|
ENST00000355773.5:c.1261T>A
|
ENSP00000348019.5:p.Tyr421Asn
|
|
NM_012434.4:c.1261T>A
|
NP_036566.1:p.Tyr421Asn
|
|
XM_005248710.2:c.1210T>A
|
XP_005248767.1:p.Tyr404Asn
|
|
XM_005248711.1:c.1063T>A
|
XP_005248768.1:p.Tyr355Asn
|
|
XM_011535750.1:c.1113T>A
|
XP_011534052.1:p.Gly371=
|
|
NM_012434.5:c.1261T>A
MANE Select
|
NP_036566.1:p.Tyr421Asn
|
|
NM_001382629.1:c.1030T>A
|
NP_001369558.1:p.Tyr344Asn
|
|
NM_001382630.1:c.1260-5226T>A
|
NP_001369559.1:n.1260-5226T>A
|
|
NM_001382631.1:c.1282T>A
|
NP_001369560.1:p.Tyr428Asn
|
|
NM_001382632.1:c.1174T>A
|
NP_001369561.1:p.Tyr392Asn
|
|
NM_001382633.1:c.1261T>A
|
NP_001369562.1:p.Tyr421Asn
|
|
NM_001382634.1:c.1102T>A
|
NP_001369563.1:p.Tyr368Asn
|
|
NM_001382635.1:c.1258T>A
|
NP_001369564.1:p.Tyr420Asn
|
|
NM_001382636.1:c.943T>A
|
NP_001369565.1:p.Tyr315Asn
|
|