ENST00000266771.10:c.575G=
MANE Select
|
ENSP00000266771.5:p.Arg192=
|
|
ENST00000266771.9:c.575G=
|
ENSP00000266771.5:p.Arg192=
|
|
ENST00000366292.6:n.887G=
|
|
|
ENST00000376740.8:c.154G=
|
|
|
ENST00000376744.8:c.411G=
|
|
|
ENST00000535272.1:n.369G=
|
|
|
ENST00000539703.1:n.225G=
|
|
|
NM_145648.3:c.575G=
|
NP_663623.1:p.Arg192=
|
|
XM_011537895.1:c.725G=
|
XP_011536197.1:p.Arg242=
|
|
XR_429081.2:n.598G=
|
|
|
XR_944494.1:n.748G=
|
|
|
XR_944495.1:n.748G=
|
|
|
XR_944496.1:n.748G=
|
|
|
XR_944497.1:n.748G=
|
|
|
XM_017018791.1:c.725G=
|
XP_016874280.1:p.Arg242=
|
|
XM_017018792.1:c.725G=
|
XP_016874281.1:p.Arg242=
|
|
XM_017018793.1:c.575G=
|
XP_016874282.1:p.Arg192=
|
|
XR_002957287.1:n.598G=
|
|
|
XR_944496.2:n.748G=
|
|
|
NM_145648.4:c.575G=
MANE Select
|
NP_663623.1:p.Arg192=
|
|