ENST00000304895.9:c.1875A>T
MANE Select
|
ENSP00000302728.4:p.Arg625Ser
|
|
ENST00000304895.8:c.1875A>T
|
ENSP00000302728.4:p.Arg625Ser
|
|
ENST00000421103.5:c.1437A>T
|
ENSP00000391390.1:p.Arg479Ser
|
|
ENST00000430730.5:c.*1142A>T
|
ENSP00000411859.1:n.*1142A>T
|
|
ENST00000447929.5:c.*1255A>T
|
ENSP00000411262.1:n.*1255A>T
|
|
ENST00000466883.5:n.2265A>T
|
|
|
NM_000181.3:c.1875A>T
|
NP_000172.2:p.Arg625Ser
|
|
NM_001284290.1:c.1437A>T
|
NP_001271219.1:p.Arg479Ser
|
|
NM_001293104.1:c.1305A>T
|
NP_001280033.1:p.Arg435Ser
|
|
NM_001293105.1:c.1218A>T
|
NP_001280034.1:p.Arg406Ser
|
|
NR_120531.1:n.1921A>T
|
|
|
XM_005250297.3:c.1722A>T
|
XP_005250354.1:p.Arg574Ser
|
|
XM_011516113.1:c.1374A>T
|
XP_011514415.1:p.Arg458Ser
|
|
XM_011516114.1:c.1203A>T
|
XP_011514416.1:p.Arg401Ser
|
|
XM_005250297.4:c.1722A>T
|
XP_005250354.1:p.Arg574Ser
|
|
XM_011516114.2:c.1203A>T
|
XP_011514416.1:p.Arg401Ser
|
|
XM_017012091.1:c.1221A>T
|
XP_016867580.1:p.Arg407Ser
|
|
XM_017012092.1:c.1152A>T
|
XP_016867581.1:p.Arg384Ser
|
|
XM_017012093.2:c.1050A>T
|
XP_016867582.1:p.Arg350Ser
|
|
XR_001744658.2:n.1682A>T
|
|
|
XR_001744659.2:n.1795A>T
|
|
|
XR_001744660.2:n.1727A>T
|
|
|
XR_001744661.2:n.1642A>T
|
|
|
XR_927461.3:n.1880A>T
|
|
|
NM_000181.4:c.1875A>T
MANE Select
|
NP_000172.2:p.Arg625Ser
|
|
NM_001284290.2:c.1437A>T
|
NP_001271219.1:p.Arg479Ser
|
|
NM_001293104.2:c.1305A>T
|
NP_001280033.1:p.Arg435Ser
|
|
NM_001293105.2:c.1218A>T
|
NP_001280034.1:p.Arg406Ser
|
|
NR_120531.2:n.1820A>T
|
|
|