ENST00000266771.10:c.559G>T
MANE Select
|
ENSP00000266771.5:p.Gly187Cys
|
|
ENST00000266771.9:c.559G>T
|
ENSP00000266771.5:p.Gly187Cys
|
|
ENST00000366292.6:n.871G>T
|
|
|
ENST00000376740.8:c.138G>T
|
|
|
ENST00000376744.8:c.395G>T
|
|
|
ENST00000535272.1:n.353G>T
|
|
|
ENST00000539703.1:n.209G>T
|
|
|
NM_145648.3:c.559G>T
|
NP_663623.1:p.Gly187Cys
|
|
XM_011537895.1:c.709G>T
|
XP_011536197.1:p.Gly237Cys
|
|
XR_429081.2:n.582G>T
|
|
|
XR_944494.1:n.732G>T
|
|
|
XR_944495.1:n.732G>T
|
|
|
XR_944496.1:n.732G>T
|
|
|
XR_944497.1:n.732G>T
|
|
|
XM_017018791.1:c.709G>T
|
XP_016874280.1:p.Gly237Cys
|
|
XM_017018792.1:c.709G>T
|
XP_016874281.1:p.Gly237Cys
|
|
XM_017018793.1:c.559G>T
|
XP_016874282.1:p.Gly187Cys
|
|
XR_002957287.1:n.582G>T
|
|
|
XR_944496.2:n.732G>T
|
|
|
NM_145648.4:c.559G>T
MANE Select
|
NP_663623.1:p.Gly187Cys
|
|