ENST00000296589.9:c.650T>G
MANE Select
|
ENSP00000296589.4:p.Val217Gly
|
|
ENST00000296589.8:c.650T>G
|
ENSP00000296589.4:p.Val217Gly
|
|
ENST00000382102.7:c.650T>G
|
ENSP00000371534.3:p.Val217Gly
|
|
ENST00000505056.1:n.452T>G
|
|
|
ENST00000509381.1:c.563-9425T>G
|
ENSP00000421100.1:n.563-9425T>G
|
|
ENST00000510600.1:c.125T>G
|
ENSP00000424010.1:p.Val42Gly
|
|
NM_001012509.3:c.650T>G
|
NP_001012527.1:p.Val217Gly
|
|
NM_001297417.2:c.563-9425T>G
|
NP_001284346.2:n.563-9425T>G
|
|
NM_016180.4:c.650T>G
|
NP_057264.3:p.Val217Gly
|
|
XM_011514051.1:c.248T>G
|
XP_011512353.1:p.Val83Gly
|
|
XM_011514052.1:c.650T>G
|
XP_011512354.1:p.Val217Gly
|
|
XR_925620.1:n.1467T>G
|
|
|
NM_016180.5:c.650T>G
MANE Select
|
NP_057264.4:p.Val217Gly
|
|
NM_001012509.4:c.650T>G
|
NP_001012527.2:p.Val217Gly
|
|
NM_001297417.3:c.563-9425T>G
|
NP_001284346.2:n.563-9425T>G
|
|
NM_001297417.4:c.563-9425T>G
|
NP_001284346.2:n.563-9425T>G
|
|