ENST00000355773.6:c.1304T>A
MANE Select
|
ENSP00000348019.5:p.Ile435Asn
|
|
ENST00000355773.5:c.1304T>A
|
ENSP00000348019.5:p.Ile435Asn
|
|
NM_012434.4:c.1304T>A
|
NP_036566.1:p.Ile435Asn
|
|
XM_005248710.2:c.1253T>A
|
XP_005248767.1:p.Ile418Asn
|
|
XM_005248711.1:c.1106T>A
|
XP_005248768.1:p.Ile369Asn
|
|
XM_011535750.1:c.1156T>A
|
XP_011534052.1:p.Phe386Ile
|
|
NM_012434.5:c.1304T>A
MANE Select
|
NP_036566.1:p.Ile435Asn
|
|
NM_001382629.1:c.1073T>A
|
NP_001369558.1:p.Ile358Asn
|
|
NM_001382630.1:c.1260-5183T>A
|
NP_001369559.1:n.1260-5183T>A
|
|
NM_001382631.1:c.1325T>A
|
NP_001369560.1:p.Ile442Asn
|
|
NM_001382632.1:c.1217T>A
|
NP_001369561.1:p.Ile406Asn
|
|
NM_001382633.1:c.1304T>A
|
NP_001369562.1:p.Ile435Asn
|
|
NM_001382634.1:c.1145T>A
|
NP_001369563.1:p.Ile382Asn
|
|
NM_001382635.1:c.1301T>A
|
NP_001369564.1:p.Ile434Asn
|
|
NM_001382636.1:c.986T>A
|
NP_001369565.1:p.Ile329Asn
|
|