|
ENST00000396420.8:c.1497C>T
(POMGNT1)
|
ENSP00000379698.4:p.Tyr499=
|
|
|
ENST00000477114.2:n.2059C>T
(POMGNT1)
|
|
|
|
ENST00000497439.6:n.1669C>T
(POMGNT1)
|
|
|
|
ENST00000684817.1:n.1857C>T
(POMGNT1)
|
|
|
|
ENST00000684898.1:n.2059C>T
(POMGNT1)
|
|
|
|
ENST00000685230.1:c.*807C>T
(POMGNT1)
|
ENSP00000510305.1:n.*807C>T
|
|
|
ENST00000685275.1:n.2044C>T
(POMGNT1)
|
|
|
|
ENST00000685444.1:c.1398C>T
(POMGNT1)
|
ENSP00000510762.1:p.Tyr466=
|
|
|
ENST00000685704.1:n.2059C>T
(POMGNT1)
|
|
|
|
ENST00000685775.1:n.3024C>T
(POMGNT1)
|
|
|
|
ENST00000685833.1:n.2375C>T
(POMGNT1)
|
|
|
|
ENST00000686252.1:n.2571C>T
(POMGNT1)
|
|
|
|
ENST00000686379.1:c.*621C>T
(POMGNT1)
|
ENSP00000508913.1:n.*621C>T
|
|
|
ENST00000686724.1:n.1669C>T
(POMGNT1)
|
|
|
|
ENST00000686737.1:c.1497C>T
(POMGNT1)
|
ENSP00000508736.1:p.Tyr499=
|
|
|
ENST00000687112.1:n.2363C>T
(POMGNT1)
|
|
|
|
ENST00000687149.1:c.1497C>T
(POMGNT1)
|
ENSP00000509745.1:p.Tyr499=
|
|
|
ENST00000687197.1:c.*437C>T
(POMGNT1)
|
ENSP00000510749.1:n.*437C>T
|
|
|
ENST00000687235.1:n.2059C>T
(POMGNT1)
|
|
|
|
ENST00000687613.1:n.2247C>T
(POMGNT1)
|
|
|
|
ENST00000687683.1:c.1497C>T
(POMGNT1)
|
ENSP00000508522.1:p.Tyr499=
|
|
|
ENST00000688032.1:n.2059C>T
(POMGNT1)
|
|
|
|
ENST00000688596.1:n.2148C>T
(POMGNT1)
|
|
|
|
ENST00000688608.1:c.1398C>T
(POMGNT1)
|
ENSP00000508890.1:p.Tyr466=
|
|
|
ENST00000688919.1:n.2693C>T
(POMGNT1)
|
|
|
|
ENST00000689031.1:n.2059C>T
(POMGNT1)
|
|
|
|
ENST00000689717.1:n.1669C>T
(POMGNT1)
|
|
|
|
ENST00000689756.1:c.*1129C>T
(POMGNT1)
|
ENSP00000509023.1:n.*1129C>T
|
|
|
ENST00000690377.1:n.1844C>T
(POMGNT1)
|
|
|
|
ENST00000690678.1:c.1497C>T
(POMGNT1)
|
ENSP00000508703.1:p.Tyr499=
|
|
|
ENST00000691209.1:c.*437C>T
(POMGNT1)
|
ENSP00000510112.1:n.*437C>T
|
|
|
ENST00000691243.1:c.1497C>T
(POMGNT1)
|
ENSP00000510654.1:p.Tyr499=
|
|
|
ENST00000692169.1:n.1646C>T
(POMGNT1)
|
|
|
|
ENST00000692202.1:n.2072C>T
(POMGNT1)
|
|
|
|
ENST00000692322.1:c.*1349C>T
(POMGNT1)
|
ENSP00000509017.1:n.*1349C>T
|
|
|
ENST00000692369.1:c.1497C>T
(POMGNT1)
|
ENSP00000508453.1:p.Tyr499=
|
|
|
ENST00000692599.1:n.2059C>T
(POMGNT1)
|
|
|
|
ENST00000692635.1:c.*437C>T
(POMGNT1)
|
ENSP00000508425.1:n.*437C>T
|
|
|
ENST00000693168.1:n.1758C>T
(POMGNT1)
|
|
|
|
ENST00000693218.1:c.1497C>T
(POMGNT1)
|
ENSP00000510577.1:p.Tyr499=
|
|
|
ENST00000693223.1:n.2445C>T
(POMGNT1)
|
|
|
|
ENST00000693365.1:n.4131C>T
(POMGNT1)
|
|
|
|
ENST00000371984.8:c.1497C>T
(POMGNT1)
MANE Select
|
ENSP00000361052.3:p.Tyr499=
|
|
|
ENST00000371984.7:c.1497C>T
(POMGNT1)
|
ENSP00000361052.3:p.Tyr499=
|
|
|
ENST00000371992.1:c.1497C>T
(POMGNT1)
|
ENSP00000361060.1:p.Tyr499=
|
|
|
ENST00000396420.7:c.*1166C>T
(POMGNT1)
|
ENSP00000379698.3:n.*1166C>T
|
|
|
ENST00000463030.1:n.118C>T
(POMGNT1)
|
|
|
|
ENST00000485714.1:n.883C>T
(POMGNT1)
|
|
|
|
NM_001243766.1:c.1497C>T
(POMGNT1)
|
NP_001230695.1:p.Tyr499=
|
|
|
NM_001290129.1:c.1431C>T
(POMGNT1)
|
NP_001277058.1:p.Tyr477=
|
|
|
NM_001290130.1:c.1068C>T
(POMGNT1)
|
NP_001277059.1:p.Tyr356=
|
|
|
NM_017739.3:c.1497C>T
(POMGNT1)
|
NP_060209.3:p.Tyr499=
|
|
|
XM_005271010.1:c.1497C>T
(POMGNT1)
|
XP_005271067.1:p.Tyr499=
|
|
|
XM_006710755.1:c.1497C>T
(POMGNT1)
|
XP_006710818.1:p.Tyr499=
|
|
|
XM_006710756.1:c.1497C>T
(POMGNT1)
|
XP_006710819.1:p.Tyr499=
|
|
|
XM_011540460.1:c.679-4062G>A
(TSPAN1)
|
XP_011538762.1:n.679-4062G>A
|
|
|
XM_011540461.1:c.634-4062G>A
(TSPAN1)
|
XP_011538763.1:n.634-4062G>A
|
|
|
XM_011541759.1:c.1431C>T
(POMGNT1)
|
XP_011540061.1:p.Tyr477=
|
|
|
XM_011541760.1:c.1431C>T
(POMGNT1)
|
XP_011540062.1:p.Tyr477=
|
|
|
XM_011541761.1:c.405C>T
(POMGNT1)
|
XP_011540063.1:p.Tyr135=
|
|
|
XR_946706.1:n.1657C>T
(POMGNT1)
|
|
|
|
XM_011540460.3:c.679-4062G>A
(TSPAN1)
|
XP_011538762.1:n.679-4062G>A
|
|
|
XM_011541760.3:c.1431C>T
(POMGNT1)
|
XP_011540062.1:p.Tyr477=
|
|
|
XM_017001690.1:c.1497C>T
(POMGNT1)
|
XP_016857179.1:p.Tyr499=
|
|
|
NM_001243766.2:c.1497C>T
(POMGNT1)
|
NP_001230695.2:p.Tyr499=
|
|
|
NM_001290129.2:c.1431C>T
(POMGNT1)
|
NP_001277058.2:p.Tyr477=
|
|
|
NM_001290130.2:c.1068C>T
(POMGNT1)
|
NP_001277059.2:p.Tyr356=
|
|
|
NM_017739.4:c.1497C>T
(POMGNT1)
MANE Select
|
NP_060209.4:p.Tyr499=
|
|
