ENST00000355773.6:c.1303A>T
MANE Select
|
ENSP00000348019.5:p.Ile435Phe
|
|
ENST00000355773.5:c.1303A>T
|
ENSP00000348019.5:p.Ile435Phe
|
|
NM_012434.4:c.1303A>T
|
NP_036566.1:p.Ile435Phe
|
|
XM_005248710.2:c.1252A>T
|
XP_005248767.1:p.Ile418Phe
|
|
XM_005248711.1:c.1105A>T
|
XP_005248768.1:p.Ile369Phe
|
|
XM_011535750.1:c.1155A>T
|
XP_011534052.1:p.Leu385=
|
|
NM_012434.5:c.1303A>T
MANE Select
|
NP_036566.1:p.Ile435Phe
|
|
NM_001382629.1:c.1072A>T
|
NP_001369558.1:p.Ile358Phe
|
|
NM_001382630.1:c.1260-5184A>T
|
NP_001369559.1:n.1260-5184A>T
|
|
NM_001382631.1:c.1324A>T
|
NP_001369560.1:p.Ile442Phe
|
|
NM_001382632.1:c.1216A>T
|
NP_001369561.1:p.Ile406Phe
|
|
NM_001382633.1:c.1303A>T
|
NP_001369562.1:p.Ile435Phe
|
|
NM_001382634.1:c.1144A>T
|
NP_001369563.1:p.Ile382Phe
|
|
NM_001382635.1:c.1300A>T
|
NP_001369564.1:p.Ile434Phe
|
|
NM_001382636.1:c.985A>T
|
NP_001369565.1:p.Ile329Phe
|
|