ENST00000350721.9:c.4447T>G
MANE Select
|
ENSP00000343741.4:p.Leu1483Val
|
|
ENST00000653868.1:n.4476T>G
|
|
|
ENST00000656590.1:c.3237T>G
|
|
|
ENST00000661310.1:c.4255T>G
|
ENSP00000499589.1:p.Leu1419Val
|
|
ENST00000350721.8:c.4447T>G
|
ENSP00000343741.4:p.Leu1483Val
|
|
NM_001184.3:c.4447T>G
|
NP_001175.2:p.Leu1483Val
|
|
XM_011512924.1:c.4453T>G
|
XP_011511226.1:p.Leu1485Val
|
|
XM_011512925.1:c.4261T>G
|
XP_011511227.1:p.Leu1421Val
|
|
XM_011512926.1:c.4453T>G
|
XP_011511228.1:p.Leu1485Val
|
|
XM_011512927.1:c.4453T>G
|
XP_011511229.1:p.Leu1485Val
|
|
XR_924147.1:n.4542T>G
|
|
|
XR_924148.1:n.4542T>G
|
|
|
XR_924149.1:n.4542T>G
|
|
|
NM_001354579.1:c.4255T>G
|
NP_001341508.1:p.Leu1419Val
|
|
XR_001740179.2:n.4536T>G
|
|
|
XR_001740180.2:n.4542T>G
|
|
|
XR_001740181.2:n.4542T>G
|
|
|
XR_001740182.1:n.4542T>G
|
|
|
XR_002959543.1:n.4542T>G
|
|
|
XR_924148.2:n.4542T>G
|
|
|
NM_001184.4:c.4447T>G
MANE Select
|
NP_001175.2:p.Leu1483Val
|
|
NM_001354579.2:c.4255T>G
|
NP_001341508.1:p.Leu1419Val
|
|