ENST00000298139.7:c.549C>T
MANE Select
|
ENSP00000298139.5:p.His183=
|
|
ENST00000650667.1:c.*163C>T
|
ENSP00000498593.1:n.*163C>T
|
|
ENST00000298139.5:c.549C>T
|
ENSP00000298139.5:p.His183=
|
|
NM_000553.4:c.549C>T , LRG_524t1:c.549C>T
|
NP_000544.2:p.His183=
|
|
XM_011544639.1:c.549C>T
|
XP_011542941.1:p.His183=
|
|
XR_949470.1:n.822C>T
|
|
|
XR_949471.1:n.822C>T
|
|
|
XR_949472.1:n.822C>T
|
|
|
NM_000553.5:c.549C>T
|
NP_000544.2:p.His183=
|
|
XM_011544639.3:c.549C>T
|
XP_011542941.1:p.His183=
|
|
XM_024447265.1:c.339C>T
|
XP_024303033.1:p.His113=
|
|
XR_949470.3:n.850C>T
|
|
|
XR_949471.3:n.850C>T
|
|
|
XR_949472.3:n.850C>T
|
|
|
NM_000553.6:c.549C>T
MANE Select
|
NP_000544.2:p.His183=
|
|