ENST00000355773.6:c.1262A>T
MANE Select
|
ENSP00000348019.5:p.Tyr421Phe
|
|
ENST00000355773.5:c.1262A>T
|
ENSP00000348019.5:p.Tyr421Phe
|
|
NM_012434.4:c.1262A>T
|
NP_036566.1:p.Tyr421Phe
|
|
XM_005248710.2:c.1211A>T
|
XP_005248767.1:p.Tyr404Phe
|
|
XM_005248711.1:c.1064A>T
|
XP_005248768.1:p.Tyr355Phe
|
|
XM_011535750.1:c.1114A>T
|
XP_011534052.1:p.Met372Leu
|
|
NM_012434.5:c.1262A>T
MANE Select
|
NP_036566.1:p.Tyr421Phe
|
|
NM_001382629.1:c.1031A>T
|
NP_001369558.1:p.Tyr344Phe
|
|
NM_001382630.1:c.1260-5225A>T
|
NP_001369559.1:n.1260-5225A>T
|
|
NM_001382631.1:c.1283A>T
|
NP_001369560.1:p.Tyr428Phe
|
|
NM_001382632.1:c.1175A>T
|
NP_001369561.1:p.Tyr392Phe
|
|
NM_001382633.1:c.1262A>T
|
NP_001369562.1:p.Tyr421Phe
|
|
NM_001382634.1:c.1103A>T
|
NP_001369563.1:p.Tyr368Phe
|
|
NM_001382635.1:c.1259A>T
|
NP_001369564.1:p.Tyr420Phe
|
|
NM_001382636.1:c.944A>T
|
NP_001369565.1:p.Tyr315Phe
|
|