ENST00000355773.6:c.1276C>G
MANE Select
|
ENSP00000348019.5:p.Leu426Val
|
|
ENST00000355773.5:c.1276C>G
|
ENSP00000348019.5:p.Leu426Val
|
|
NM_012434.4:c.1276C>G
|
NP_036566.1:p.Leu426Val
|
|
XM_005248710.2:c.1225C>G
|
XP_005248767.1:p.Leu409Val
|
|
XM_005248711.1:c.1078C>G
|
XP_005248768.1:p.Leu360Val
|
|
XM_011535750.1:c.1128C>G
|
XP_011534052.1:p.Ser376=
|
|
NM_012434.5:c.1276C>G
MANE Select
|
NP_036566.1:p.Leu426Val
|
|
NM_001382629.1:c.1045C>G
|
NP_001369558.1:p.Leu349Val
|
|
NM_001382630.1:c.1260-5211C>G
|
NP_001369559.1:n.1260-5211C>G
|
|
NM_001382631.1:c.1297C>G
|
NP_001369560.1:p.Leu433Val
|
|
NM_001382632.1:c.1189C>G
|
NP_001369561.1:p.Leu397Val
|
|
NM_001382633.1:c.1276C>G
|
NP_001369562.1:p.Leu426Val
|
|
NM_001382634.1:c.1117C>G
|
NP_001369563.1:p.Leu373Val
|
|
NM_001382635.1:c.1273C>G
|
NP_001369564.1:p.Leu425Val
|
|
NM_001382636.1:c.958C>G
|
NP_001369565.1:p.Leu320Val
|
|