ENST00000355773.6:c.1339C>G
MANE Select
|
ENSP00000348019.5:p.Leu447Val
|
|
ENST00000355773.5:c.1339C>G
|
ENSP00000348019.5:p.Leu447Val
|
|
NM_012434.4:c.1339C>G
|
NP_036566.1:p.Leu447Val
|
|
XM_005248710.2:c.1288C>G
|
XP_005248767.1:p.Leu430Val
|
|
XM_005248711.1:c.1141C>G
|
XP_005248768.1:p.Leu381Val
|
|
XM_011535750.1:c.1191C>G
|
XP_011534052.1:p.Val397=
|
|
NM_012434.5:c.1339C>G
MANE Select
|
NP_036566.1:p.Leu447Val
|
|
NM_001382629.1:c.1108C>G
|
NP_001369558.1:p.Leu370Val
|
|
NM_001382630.1:c.1260-5148C>G
|
NP_001369559.1:n.1260-5148C>G
|
|
NM_001382631.1:c.1360C>G
|
NP_001369560.1:p.Leu454Val
|
|
NM_001382632.1:c.1252C>G
|
NP_001369561.1:p.Leu418Val
|
|
NM_001382633.1:c.1339C>G
|
NP_001369562.1:p.Leu447Val
|
|
NM_001382634.1:c.1180C>G
|
NP_001369563.1:p.Leu394Val
|
|
NM_001382635.1:c.1336C>G
|
NP_001369564.1:p.Leu446Val
|
|
NM_001382636.1:c.1021C>G
|
NP_001369565.1:p.Leu341Val
|
|