ENST00000304895.9:c.1806G>T
MANE Select
|
ENSP00000302728.4:p.Leu602=
|
|
ENST00000304895.8:c.1806G>T
|
ENSP00000302728.4:p.Leu602=
|
|
ENST00000421103.5:c.1368G>T
|
ENSP00000391390.1:p.Leu456=
|
|
ENST00000430730.5:c.*1073G>T
|
ENSP00000411859.1:n.*1073G>T
|
|
ENST00000447929.5:c.*1186G>T
|
ENSP00000411262.1:n.*1186G>T
|
|
ENST00000466883.5:n.2196G>T
|
|
|
NM_000181.3:c.1806G>T
|
NP_000172.2:p.Leu602=
|
|
NM_001284290.1:c.1368G>T
|
NP_001271219.1:p.Leu456=
|
|
NM_001293104.1:c.1236G>T
|
NP_001280033.1:p.Leu412=
|
|
NM_001293105.1:c.1149G>T
|
NP_001280034.1:p.Leu383=
|
|
NR_120531.1:n.1852G>T
|
|
|
XM_005250297.3:c.1653G>T
|
XP_005250354.1:p.Leu551=
|
|
XM_011516113.1:c.1305G>T
|
XP_011514415.1:p.Leu435=
|
|
XM_011516114.1:c.1134G>T
|
XP_011514416.1:p.Leu378=
|
|
XM_005250297.4:c.1653G>T
|
XP_005250354.1:p.Leu551=
|
|
XM_011516114.2:c.1134G>T
|
XP_011514416.1:p.Leu378=
|
|
XM_017012091.1:c.1152G>T
|
XP_016867580.1:p.Leu384=
|
|
XM_017012092.1:c.1083G>T
|
XP_016867581.1:p.Leu361=
|
|
XM_017012093.2:c.981G>T
|
XP_016867582.1:p.Leu327=
|
|
XR_001744658.2:n.1613G>T
|
|
|
XR_001744659.2:n.1726G>T
|
|
|
XR_001744660.2:n.1658G>T
|
|
|
XR_001744661.2:n.1573G>T
|
|
|
XR_927461.3:n.1811G>T
|
|
|
NM_000181.4:c.1806G>T
MANE Select
|
NP_000172.2:p.Leu602=
|
|
NM_001284290.2:c.1368G>T
|
NP_001271219.1:p.Leu456=
|
|
NM_001293104.2:c.1236G>T
|
NP_001280033.1:p.Leu412=
|
|
NM_001293105.2:c.1149G>T
|
NP_001280034.1:p.Leu383=
|
|
NR_120531.2:n.1751G>T
|
|
|