ENST00000348931.9:c.532T>G
MANE Select
|
ENSP00000335384.5:p.Leu178Val
|
|
ENST00000348931.8:c.532T>G
|
ENSP00000335384.5:p.Leu178Val
|
|
ENST00000377940.3:c.466T>G
|
ENSP00000367174.3:p.Leu156Val
|
|
ENST00000583811.5:c.178T>G
|
ENSP00000462463.1:p.Leu60Val
|
|
ENST00000584588.5:c.407-649T>G
|
ENSP00000462067.1:n.407-649T>G
|
|
NM_198844.2:c.466T>G
|
NP_942141.2:p.Leu156Val
|
|
NM_199321.2:c.532T>G
|
NP_955353.1:p.Leu178Val
|
|
XM_011524298.1:c.532T>G
|
XP_011522600.1:p.Leu178Val
|
|
XR_002957959.1:n.723T>G
|
|
|
NM_198844.3:c.466T>G
|
NP_942141.2:p.Leu156Val
|
|
NM_199321.3:c.532T>G
MANE Select
|
NP_955353.1:p.Leu178Val
|
|