ENST00000380044.6:c.482T>G
MANE Select
|
ENSP00000369383.1:p.Val161Gly
|
|
ENST00000233545.6:c.482T>G
|
ENSP00000233545.2:p.Val161Gly
|
|
ENST00000357186.10:c.314T>G
|
ENSP00000349713.6:p.Val105Gly
|
|
ENST00000380044.5:c.482T>G
|
ENSP00000369383.1:p.Val161Gly
|
|
ENST00000402310.5:c.429T>G
|
ENSP00000383955.1:p.Cys143Trp
|
|
ENST00000402722.5:c.*61T>G
|
ENSP00000386000.1:n.*61T>G
|
|
ENST00000405076.5:c.293T>G
|
ENSP00000385175.1:p.Val98Gly
|
|
ENST00000405983.5:c.527T>G
|
ENSP00000384586.1:p.Val176Gly
|
|
ENST00000415514.5:c.*283T>G
|
ENSP00000388043.1:n.*283T>G
|
|
ENST00000426513.6:c.*147T>G
|
ENSP00000403824.2:n.*147T>G
|
|
ENST00000430991.5:c.316T>G
|
|
|
ENST00000620797.4:n.155T>G
|
|
|
ENST00000621183.4:n.785T>G
|
|
|
NM_002437.4:c.482T>G
|
NP_002428.1:p.Val161Gly
|
|
XM_005264326.2:c.482T>G
|
XP_005264383.1:p.Val161Gly
|
|
XM_005264327.2:c.323T>G
|
XP_005264384.1:p.Val108Gly
|
|
XM_006712021.2:c.434T>G
|
XP_006712084.1:p.Val145Gly
|
|
XM_005264326.4:c.482T>G
|
XP_005264383.1:p.Val161Gly
|
|
XM_006712021.3:c.434T>G
|
XP_006712084.1:p.Val145Gly
|
|
XM_017004150.1:c.464T>G
|
XP_016859639.1:p.Val155Gly
|
|
XM_017004151.1:c.434T>G
|
XP_016859640.1:p.Val145Gly
|
|
XM_017004152.1:c.323T>G
|
XP_016859641.1:p.Val108Gly
|
|
XM_024452913.1:c.434T>G
|
XP_024308681.1:p.Val145Gly
|
|
NM_002437.5:c.482T>G
MANE Select
|
NP_002428.1:p.Val161Gly
|
|