ENST00000355773.6:c.1263T>A
MANE Select
|
ENSP00000348019.5:p.Tyr421Ter
|
|
ENST00000355773.5:c.1263T>A
|
ENSP00000348019.5:p.Tyr421Ter
|
|
NM_012434.4:c.1263T>A
|
NP_036566.1:p.Tyr421Ter
|
|
XM_005248710.2:c.1212T>A
|
XP_005248767.1:p.Tyr404Ter
|
|
XM_005248711.1:c.1065T>A
|
XP_005248768.1:p.Tyr355Ter
|
|
XM_011535750.1:c.1115T>A
|
XP_011534052.1:p.Met372Lys
|
|
NM_012434.5:c.1263T>A
MANE Select
|
NP_036566.1:p.Tyr421Ter
|
|
NM_001382629.1:c.1032T>A
|
NP_001369558.1:p.Tyr344Ter
|
|
NM_001382630.1:c.1260-5224T>A
|
NP_001369559.1:n.1260-5224T>A
|
|
NM_001382631.1:c.1284T>A
|
NP_001369560.1:p.Tyr428Ter
|
|
NM_001382632.1:c.1176T>A
|
NP_001369561.1:p.Tyr392Ter
|
|
NM_001382633.1:c.1263T>A
|
NP_001369562.1:p.Tyr421Ter
|
|
NM_001382634.1:c.1104T>A
|
NP_001369563.1:p.Tyr368Ter
|
|
NM_001382635.1:c.1260T>A
|
NP_001369564.1:p.Tyr420Ter
|
|
NM_001382636.1:c.945T>A
|
NP_001369565.1:p.Tyr315Ter
|
|