ENST00000355773.6:c.1304T>G
MANE Select
|
ENSP00000348019.5:p.Ile435Ser
|
|
ENST00000355773.5:c.1304T>G
|
ENSP00000348019.5:p.Ile435Ser
|
|
NM_012434.4:c.1304T>G
|
NP_036566.1:p.Ile435Ser
|
|
XM_005248710.2:c.1253T>G
|
XP_005248767.1:p.Ile418Ser
|
|
XM_005248711.1:c.1106T>G
|
XP_005248768.1:p.Ile369Ser
|
|
XM_011535750.1:c.1156T>G
|
XP_011534052.1:p.Phe386Val
|
|
NM_012434.5:c.1304T>G
MANE Select
|
NP_036566.1:p.Ile435Ser
|
|
NM_001382629.1:c.1073T>G
|
NP_001369558.1:p.Ile358Ser
|
|
NM_001382630.1:c.1260-5183T>G
|
NP_001369559.1:n.1260-5183T>G
|
|
NM_001382631.1:c.1325T>G
|
NP_001369560.1:p.Ile442Ser
|
|
NM_001382632.1:c.1217T>G
|
NP_001369561.1:p.Ile406Ser
|
|
NM_001382633.1:c.1304T>G
|
NP_001369562.1:p.Ile435Ser
|
|
NM_001382634.1:c.1145T>G
|
NP_001369563.1:p.Ile382Ser
|
|
NM_001382635.1:c.1301T>G
|
NP_001369564.1:p.Ile434Ser
|
|
NM_001382636.1:c.986T>G
|
NP_001369565.1:p.Ile329Ser
|
|