ENST00000304895.9:c.1838G>T
MANE Select
|
ENSP00000302728.4:p.Arg613Ile
|
|
ENST00000304895.8:c.1838G>T
|
ENSP00000302728.4:p.Arg613Ile
|
|
ENST00000421103.5:c.1400G>T
|
ENSP00000391390.1:p.Arg467Ile
|
|
ENST00000430730.5:c.*1105G>T
|
ENSP00000411859.1:n.*1105G>T
|
|
ENST00000447929.5:c.*1218G>T
|
ENSP00000411262.1:n.*1218G>T
|
|
ENST00000466883.5:n.2228G>T
|
|
|
NM_000181.3:c.1838G>T
|
NP_000172.2:p.Arg613Ile
|
|
NM_001284290.1:c.1400G>T
|
NP_001271219.1:p.Arg467Ile
|
|
NM_001293104.1:c.1268G>T
|
NP_001280033.1:p.Arg423Ile
|
|
NM_001293105.1:c.1181G>T
|
NP_001280034.1:p.Arg394Ile
|
|
NR_120531.1:n.1884G>T
|
|
|
XM_005250297.3:c.1685G>T
|
XP_005250354.1:p.Arg562Ile
|
|
XM_011516113.1:c.1337G>T
|
XP_011514415.1:p.Arg446Ile
|
|
XM_011516114.1:c.1166G>T
|
XP_011514416.1:p.Arg389Ile
|
|
XM_005250297.4:c.1685G>T
|
XP_005250354.1:p.Arg562Ile
|
|
XM_011516114.2:c.1166G>T
|
XP_011514416.1:p.Arg389Ile
|
|
XM_017012091.1:c.1184G>T
|
XP_016867580.1:p.Arg395Ile
|
|
XM_017012092.1:c.1115G>T
|
XP_016867581.1:p.Arg372Ile
|
|
XM_017012093.2:c.1013G>T
|
XP_016867582.1:p.Arg338Ile
|
|
XR_001744658.2:n.1645G>T
|
|
|
XR_001744659.2:n.1758G>T
|
|
|
XR_001744660.2:n.1690G>T
|
|
|
XR_001744661.2:n.1605G>T
|
|
|
XR_927461.3:n.1843G>T
|
|
|
NM_000181.4:c.1838G>T
MANE Select
|
NP_000172.2:p.Arg613Ile
|
|
NM_001284290.2:c.1400G>T
|
NP_001271219.1:p.Arg467Ile
|
|
NM_001293104.2:c.1268G>T
|
NP_001280033.1:p.Arg423Ile
|
|
NM_001293105.2:c.1181G>T
|
NP_001280034.1:p.Arg394Ile
|
|
NR_120531.2:n.1783G>T
|
|
|