ENST00000317961.9:c.3712C>T
MANE Select
|
ENSP00000322408.4:p.Arg1238Ter
|
|
ENST00000317961.8:c.3712C>T
|
ENSP00000322408.4:p.Arg1238Ter
|
|
ENST00000382806.6:c.3541C>T
|
ENSP00000372256.2:p.Arg1181Ter
|
|
ENST00000415360.1:c.628C>T
|
ENSP00000389433.1:p.Arg210Ter
|
|
ENST00000440077.5:c.3589C>T
|
ENSP00000398543.1:p.Arg1197Ter
|
|
ENST00000469599.6:n.2310C>T
|
|
|
ENST00000492117.1:n.3604C>T
|
|
|
ENST00000541639.5:c.3805C>T
|
ENSP00000444293.1:p.Arg1269Ter
|
|
NM_001146705.1:c.3805C>T
|
NP_001140177.1:p.Arg1269Ter
|
|
NM_001146706.1:c.3541C>T
|
NP_001140178.1:p.Arg1181Ter
|
|
NM_004653.4:c.3712C>T
|
NP_004644.2:p.Arg1238Ter
|
|
XM_005262560.1:c.3577C>T
|
XP_005262617.1:p.Arg1193Ter
|
|
XM_005262561.1:c.3481C>T
|
XP_005262618.1:p.Arg1161Ter
|
|
XM_011531468.1:c.3634C>T
|
XP_011529770.1:p.Arg1212Ter
|
|
XR_244571.2:n.4000C>T
|
|
|
XR_430568.2:n.4334C>T
|
|
|
XM_005262560.3:c.3577C>T
|
XP_005262617.1:p.Arg1193Ter
|
|
XM_005262561.3:c.3481C>T
|
XP_005262618.1:p.Arg1161Ter
|
|
XM_011531468.3:c.3634C>T
|
XP_011529770.1:p.Arg1212Ter
|
|
XM_024452495.1:c.1702C>T
|
XP_024308263.1:p.Arg568Ter
|
|
XM_024452496.1:c.1468C>T
|
XP_024308264.1:p.Arg490Ter
|
|
XR_001756009.2:n.4450C>T
|
|
|
XR_001756010.2:n.4450C>T
|
|
|
XR_001756011.2:n.4315C>T
|
|
|
XR_001756012.2:n.4463C>T
|
|
|
XR_001756013.2:n.3781C>T
|
|
|
XR_002958832.1:n.3882C>T
|
|
|
XR_002958834.1:n.4106C>T
|
|
|
XR_002958835.1:n.3989C>T
|
|
|
XR_002958836.1:n.4672C>T
|
|
|
XR_002958837.1:n.4479C>T
|
|
|
XR_244571.4:n.3999C>T
|
|
|
XR_430568.4:n.4333C>T
|
|
|
NM_001146706.2:c.3541C>T
|
NP_001140178.1:p.Arg1181Ter
|
|
NM_004653.5:c.3712C>T
MANE Select
|
NP_004644.2:p.Arg1238Ter
|
|
NM_001146705.2:c.3805C>T
|
NP_001140177.1:p.Arg1269Ter
|
|