ENST00000304895.9:c.1808G>T
MANE Select
|
ENSP00000302728.4:p.Gly603Val
|
|
ENST00000304895.8:c.1808G>T
|
ENSP00000302728.4:p.Gly603Val
|
|
ENST00000421103.5:c.1370G>T
|
ENSP00000391390.1:p.Gly457Val
|
|
ENST00000430730.5:c.*1075G>T
|
ENSP00000411859.1:n.*1075G>T
|
|
ENST00000447929.5:c.*1188G>T
|
ENSP00000411262.1:n.*1188G>T
|
|
ENST00000466883.5:n.2198G>T
|
|
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NM_000181.3:c.1808G>T
|
NP_000172.2:p.Gly603Val
|
|
NM_001284290.1:c.1370G>T
|
NP_001271219.1:p.Gly457Val
|
|
NM_001293104.1:c.1238G>T
|
NP_001280033.1:p.Gly413Val
|
|
NM_001293105.1:c.1151G>T
|
NP_001280034.1:p.Gly384Val
|
|
NR_120531.1:n.1854G>T
|
|
|
XM_005250297.3:c.1655G>T
|
XP_005250354.1:p.Gly552Val
|
|
XM_011516113.1:c.1307G>T
|
XP_011514415.1:p.Gly436Val
|
|
XM_011516114.1:c.1136G>T
|
XP_011514416.1:p.Gly379Val
|
|
XM_005250297.4:c.1655G>T
|
XP_005250354.1:p.Gly552Val
|
|
XM_011516114.2:c.1136G>T
|
XP_011514416.1:p.Gly379Val
|
|
XM_017012091.1:c.1154G>T
|
XP_016867580.1:p.Gly385Val
|
|
XM_017012092.1:c.1085G>T
|
XP_016867581.1:p.Gly362Val
|
|
XM_017012093.2:c.983G>T
|
XP_016867582.1:p.Gly328Val
|
|
XR_001744658.2:n.1615G>T
|
|
|
XR_001744659.2:n.1728G>T
|
|
|
XR_001744660.2:n.1660G>T
|
|
|
XR_001744661.2:n.1575G>T
|
|
|
XR_927461.3:n.1813G>T
|
|
|
NM_000181.4:c.1808G>T
MANE Select
|
NP_000172.2:p.Gly603Val
|
|
NM_001284290.2:c.1370G>T
|
NP_001271219.1:p.Gly457Val
|
|
NM_001293104.2:c.1238G>T
|
NP_001280033.1:p.Gly413Val
|
|
NM_001293105.2:c.1151G>T
|
NP_001280034.1:p.Gly384Val
|
|
NR_120531.2:n.1753G>T
|
|
|