ENST00000400521.7:c.1132C>G
MANE Select
|
ENSP00000383365.1:p.Leu378Val
|
|
ENST00000400518.5:c.1042C>G
|
ENSP00000383362.1:p.Leu348Val
|
|
ENST00000400519.6:c.1129C>G
|
ENSP00000383363.1:p.Leu377Val
|
|
ENST00000400521.6:c.1132C>G
|
ENSP00000383365.1:p.Leu378Val
|
|
ENST00000400525.6:c.1063C>G
|
ENSP00000383369.3:p.Leu355Val
|
|
ENST00000462330.5:c.55C>G
|
ENSP00000485603.2:p.Leu19Val
|
|
ENST00000462843.2:c.82C>G
|
ENSP00000485466.2:p.Leu28Val
|
|
ENST00000474308.5:c.1075C>G
|
ENSP00000485665.1:p.Leu359Val
|
|
ENST00000485358.5:c.100C>G
|
ENSP00000485499.2:p.Leu34Val
|
|
ENST00000487165.5:n.1226C>G
|
|
|
ENST00000494454.5:n.1206C>G
|
|
|
ENST00000495655.2:n.676C>G
|
|
|
ENST00000542719.6:c.844C>G
|
ENSP00000485128.2:p.Leu282Val
|
|
ENST00000634471.1:n.244-401C>G
|
|
|
ENST00000634537.1:c.361C>G
|
ENSP00000489208.1:p.Leu121Val
|
|
NM_006440.4:c.1132C>G
|
NP_006431.2:p.Leu378Val
|
|
NM_001352300.1:c.1129C>G
|
NP_001339229.1:p.Leu377Val
|
|
NM_001352301.1:c.1042C>G
|
NP_001339230.1:p.Leu348Val
|
|
NM_001352302.1:c.844C>G
|
NP_001339231.1:p.Leu282Val
|
|
NR_147957.1:n.1264C>G
|
|
|
NM_006440.5:c.1132C>G
MANE Select
|
NP_006431.2:p.Leu378Val
|
|
NM_001352300.2:c.1129C>G
|
NP_001339229.1:p.Leu377Val
|
|
NR_147957.2:n.1090C>G
|
|
|
NM_001352301.2:c.1042C>G
|
NP_001339230.1:p.Leu348Val
|
|
NM_001352302.2:c.844C>G
|
NP_001339231.1:p.Leu282Val
|
|