ENST00000304895.9:c.1822A>G
MANE Select
|
ENSP00000302728.4:p.Ile608Val
|
|
ENST00000304895.8:c.1822A>G
|
ENSP00000302728.4:p.Ile608Val
|
|
ENST00000421103.5:c.1384A>G
|
ENSP00000391390.1:p.Ile462Val
|
|
ENST00000430730.5:c.*1089A>G
|
ENSP00000411859.1:n.*1089A>G
|
|
ENST00000447929.5:c.*1202A>G
|
ENSP00000411262.1:n.*1202A>G
|
|
ENST00000466883.5:n.2212A>G
|
|
|
NM_000181.3:c.1822A>G
|
NP_000172.2:p.Ile608Val
|
|
NM_001284290.1:c.1384A>G
|
NP_001271219.1:p.Ile462Val
|
|
NM_001293104.1:c.1252A>G
|
NP_001280033.1:p.Ile418Val
|
|
NM_001293105.1:c.1165A>G
|
NP_001280034.1:p.Ile389Val
|
|
NR_120531.1:n.1868A>G
|
|
|
XM_005250297.3:c.1669A>G
|
XP_005250354.1:p.Ile557Val
|
|
XM_011516113.1:c.1321A>G
|
XP_011514415.1:p.Ile441Val
|
|
XM_011516114.1:c.1150A>G
|
XP_011514416.1:p.Ile384Val
|
|
XM_005250297.4:c.1669A>G
|
XP_005250354.1:p.Ile557Val
|
|
XM_011516114.2:c.1150A>G
|
XP_011514416.1:p.Ile384Val
|
|
XM_017012091.1:c.1168A>G
|
XP_016867580.1:p.Ile390Val
|
|
XM_017012092.1:c.1099A>G
|
XP_016867581.1:p.Ile367Val
|
|
XM_017012093.2:c.997A>G
|
XP_016867582.1:p.Ile333Val
|
|
XR_001744658.2:n.1629A>G
|
|
|
XR_001744659.2:n.1742A>G
|
|
|
XR_001744660.2:n.1674A>G
|
|
|
XR_001744661.2:n.1589A>G
|
|
|
XR_927461.3:n.1827A>G
|
|
|
NM_000181.4:c.1822A>G
MANE Select
|
NP_000172.2:p.Ile608Val
|
|
NM_001284290.2:c.1384A>G
|
NP_001271219.1:p.Ile462Val
|
|
NM_001293104.2:c.1252A>G
|
NP_001280033.1:p.Ile418Val
|
|
NM_001293105.2:c.1165A>G
|
NP_001280034.1:p.Ile389Val
|
|
NR_120531.2:n.1767A>G
|
|
|