ENST00000304895.9:c.1850G=
MANE Select
|
ENSP00000302728.4:p.Ser617=
|
|
ENST00000304895.8:c.1850G=
|
ENSP00000302728.4:p.Ser617=
|
|
ENST00000421103.5:c.1412G=
|
ENSP00000391390.1:p.Ser471=
|
|
ENST00000430730.5:c.*1117G=
|
ENSP00000411859.1:n.*1117G=
|
|
ENST00000447929.5:c.*1230G=
|
ENSP00000411262.1:n.*1230G=
|
|
ENST00000466883.5:n.2240G=
|
|
|
NM_000181.3:c.1850G=
|
NP_000172.2:p.Ser617=
|
|
NM_001284290.1:c.1412G=
|
NP_001271219.1:p.Ser471=
|
|
NM_001293104.1:c.1280G=
|
NP_001280033.1:p.Ser427=
|
|
NM_001293105.1:c.1193G=
|
NP_001280034.1:p.Ser398=
|
|
NR_120531.1:n.1896G=
|
|
|
XM_005250297.3:c.1697G=
|
XP_005250354.1:p.Ser566=
|
|
XM_011516113.1:c.1349G=
|
XP_011514415.1:p.Ser450=
|
|
XM_011516114.1:c.1178G=
|
XP_011514416.1:p.Ser393=
|
|
XM_005250297.4:c.1697G=
|
XP_005250354.1:p.Ser566=
|
|
XM_011516114.2:c.1178G=
|
XP_011514416.1:p.Ser393=
|
|
XM_017012091.1:c.1196G=
|
XP_016867580.1:p.Ser399=
|
|
XM_017012092.1:c.1127G=
|
XP_016867581.1:p.Ser376=
|
|
XM_017012093.2:c.1025G=
|
XP_016867582.1:p.Ser342=
|
|
XR_001744658.2:n.1657G=
|
|
|
XR_001744659.2:n.1770G=
|
|
|
XR_001744660.2:n.1702G=
|
|
|
XR_001744661.2:n.1617G=
|
|
|
XR_927461.3:n.1855G=
|
|
|
NM_000181.4:c.1850G=
MANE Select
|
NP_000172.2:p.Ser617=
|
|
NM_001284290.2:c.1412G=
|
NP_001271219.1:p.Ser471=
|
|
NM_001293104.2:c.1280G=
|
NP_001280033.1:p.Ser427=
|
|
NM_001293105.2:c.1193G=
|
NP_001280034.1:p.Ser398=
|
|
NR_120531.2:n.1795G=
|
|
|