ENST00000253122.10:c.1357C>G
MANE Select
|
ENSP00000253122.5:p.Leu453Val
|
|
ENST00000253122.9:c.1357C>G
|
ENSP00000253122.5:p.Leu453Val
|
|
ENST00000413787.1:c.286C>G
|
ENSP00000400463.1:p.Leu96Val
|
|
ENST00000430077.6:c.1012C>G
|
ENSP00000403041.2:p.Leu338Val
|
|
ENST00000442457.1:c.411C>G
|
|
|
ENST00000485324.1:n.1502C>G
|
|
|
NM_001142805.1:c.1327C>G
|
NP_001136277.1:p.Leu443Val
|
|
NM_001142806.1:c.1012C>G
|
NP_001136278.1:p.Leu338Val
|
|
NM_005629.3:c.1357C>G
|
NP_005620.1:p.Leu453Val
|
|
NM_005629.4:c.1357C>G
MANE Select
|
NP_005620.1:p.Leu453Val
|
|
NM_001142805.2:c.1327C>G
|
NP_001136277.1:p.Leu443Val
|
|