ENST00000298139.7:c.3499C>G
MANE Select
|
ENSP00000298139.5:p.His1167Asp
|
|
ENST00000650667.1:c.*3113C>G
|
ENSP00000498593.1:n.*3113C>G
|
|
ENST00000298139.5:c.3499C>G
|
ENSP00000298139.5:p.His1167Asp
|
|
ENST00000521620.5:n.2132C>G
|
|
|
NM_000553.4:c.3499C>G , LRG_524t1:c.3499C>G
|
NP_000544.2:p.His1167Asp
|
|
XM_011544639.1:c.3418C>G
|
XP_011542941.1:p.His1140Asp
|
|
XM_011544640.1:c.1900C>G
|
XP_011542942.1:p.His634Asp
|
|
XR_949470.1:n.3772C>G
|
|
|
XR_949471.1:n.3772C>G
|
|
|
XR_949472.1:n.3772C>G
|
|
|
XR_949643.1:n.614+1105G>C
|
|
|
NM_000553.5:c.3499C>G
|
NP_000544.2:p.His1167Asp
|
|
XM_011544639.3:c.3418C>G
|
XP_011542941.1:p.His1140Asp
|
|
XM_024447265.1:c.3289C>G
|
XP_024303033.1:p.His1097Asp
|
|
XR_949470.3:n.3800C>G
|
|
|
XR_949471.3:n.3800C>G
|
|
|
XR_949472.3:n.3800C>G
|
|
|
NM_000553.6:c.3499C>G
MANE Select
|
NP_000544.2:p.His1167Asp
|
|