ENST00000355773.6:c.1329T>C
MANE Select
|
ENSP00000348019.5:p.Ile443=
|
|
ENST00000355773.5:c.1329T>C
|
ENSP00000348019.5:p.Ile443=
|
|
NM_012434.4:c.1329T>C
|
NP_036566.1:p.Ile443=
|
|
XM_005248710.2:c.1278T>C
|
XP_005248767.1:p.Ile426=
|
|
XM_005248711.1:c.1131T>C
|
XP_005248768.1:p.Ile377=
|
|
XM_011535750.1:c.1181T>C
|
XP_011534052.1:p.Leu394Ser
|
|
NM_012434.5:c.1329T>C
MANE Select
|
NP_036566.1:p.Ile443=
|
|
NM_001382629.1:c.1098T>C
|
NP_001369558.1:p.Ile366=
|
|
NM_001382630.1:c.1260-5158T>C
|
NP_001369559.1:n.1260-5158T>C
|
|
NM_001382631.1:c.1350T>C
|
NP_001369560.1:p.Ile450=
|
|
NM_001382632.1:c.1242T>C
|
NP_001369561.1:p.Ile414=
|
|
NM_001382633.1:c.1329T>C
|
NP_001369562.1:p.Ile443=
|
|
NM_001382634.1:c.1170T>C
|
NP_001369563.1:p.Ile390=
|
|
NM_001382635.1:c.1326T>C
|
NP_001369564.1:p.Ile442=
|
|
NM_001382636.1:c.1011T>C
|
NP_001369565.1:p.Ile337=
|
|