ENST00000304895.9:c.1866G>T
MANE Select
|
ENSP00000302728.4:p.Leu622Phe
|
|
ENST00000304895.8:c.1866G>T
|
ENSP00000302728.4:p.Leu622Phe
|
|
ENST00000421103.5:c.1428G>T
|
ENSP00000391390.1:p.Leu476Phe
|
|
ENST00000430730.5:c.*1133G>T
|
ENSP00000411859.1:n.*1133G>T
|
|
ENST00000447929.5:c.*1246G>T
|
ENSP00000411262.1:n.*1246G>T
|
|
ENST00000466883.5:n.2256G>T
|
|
|
NM_000181.3:c.1866G>T
|
NP_000172.2:p.Leu622Phe
|
|
NM_001284290.1:c.1428G>T
|
NP_001271219.1:p.Leu476Phe
|
|
NM_001293104.1:c.1296G>T
|
NP_001280033.1:p.Leu432Phe
|
|
NM_001293105.1:c.1209G>T
|
NP_001280034.1:p.Leu403Phe
|
|
NR_120531.1:n.1912G>T
|
|
|
XM_005250297.3:c.1713G>T
|
XP_005250354.1:p.Leu571Phe
|
|
XM_011516113.1:c.1365G>T
|
XP_011514415.1:p.Leu455Phe
|
|
XM_011516114.1:c.1194G>T
|
XP_011514416.1:p.Leu398Phe
|
|
XM_005250297.4:c.1713G>T
|
XP_005250354.1:p.Leu571Phe
|
|
XM_011516114.2:c.1194G>T
|
XP_011514416.1:p.Leu398Phe
|
|
XM_017012091.1:c.1212G>T
|
XP_016867580.1:p.Leu404Phe
|
|
XM_017012092.1:c.1143G>T
|
XP_016867581.1:p.Leu381Phe
|
|
XM_017012093.2:c.1041G>T
|
XP_016867582.1:p.Leu347Phe
|
|
XR_001744658.2:n.1673G>T
|
|
|
XR_001744659.2:n.1786G>T
|
|
|
XR_001744660.2:n.1718G>T
|
|
|
XR_001744661.2:n.1633G>T
|
|
|
XR_927461.3:n.1871G>T
|
|
|
NM_000181.4:c.1866G>T
MANE Select
|
NP_000172.2:p.Leu622Phe
|
|
NM_001284290.2:c.1428G>T
|
NP_001271219.1:p.Leu476Phe
|
|
NM_001293104.2:c.1296G>T
|
NP_001280033.1:p.Leu432Phe
|
|
NM_001293105.2:c.1209G>T
|
NP_001280034.1:p.Leu403Phe
|
|
NR_120531.2:n.1811G>T
|
|
|