ENST00000391944.8:c.1442T>G
|
ENSP00000375808.4:p.Phe481Cys
|
|
ENST00000682414.1:c.1442T>G
|
ENSP00000507019.1:p.Phe481Cys
|
|
ENST00000682508.1:n.1471T>G
|
|
|
ENST00000684218.1:c.*700T>G
|
ENSP00000507804.1:n.*700T>G
|
|
ENST00000684264.1:n.998T>G
|
|
|
ENST00000684407.1:c.1319T>G
|
ENSP00000507775.1:p.Phe440Cys
|
|
ENST00000684458.1:c.1372T>G
|
ENSP00000508260.1:p.Ser458Ala
|
|
ENST00000684468.1:n.1218T>G
|
|
|
ENST00000391945.10:c.1442T>G
MANE Select
|
ENSP00000375809.4:p.Phe481Cys
|
|
ENST00000587376.6:c.565T>G
|
|
|
ENST00000646507.1:n.1539T>G
|
|
|
ENST00000391941.6:c.1370T>G
|
ENSP00000375805.2:p.Phe457Cys
|
|
ENST00000391942.6:n.613T>G
|
|
|
ENST00000391944.7:c.1208T>G
|
ENSP00000375808.3:p.Phe403Cys
|
|
ENST00000391945.8:c.1442T>G
|
ENSP00000375809.3:p.Phe481Cys
|
|
ENST00000587376.5:c.565T>G
|
|
|
ENST00000588652.5:n.1530T>G
|
|
|
NM_000400.3:c.1442T>G , LRG_461t1:c.1442T>G
|
NP_000391.1:p.Phe481Cys
|
|
XM_011526611.1:c.1364T>G
|
XP_011524913.1:p.Phe455Cys
|
|
XR_935763.1:n.1489T>G
|
|
|
XM_011526611.2:c.1364T>G
|
XP_011524913.1:p.Phe455Cys
|
|
XM_017026467.1:c.1319T>G
|
XP_016881956.1:p.Phe440Cys
|
|
XR_001753633.2:n.1489T>G
|
|
|
XR_001753634.2:n.1489T>G
|
|
|
NM_000400.4:c.1442T>G
MANE Select
|
NP_000391.1:p.Phe481Cys
|
|