|
ENST00000222823.9:c.1060C>T
MANE Select
|
ENSP00000222823.4:p.Pro354Ser
|
|
|
ENST00000222823.8:c.1060C>T
|
ENSP00000222823.4:p.Pro354Ser
|
|
|
ENST00000434755.5:c.1060C>T
|
ENSP00000416946.1:p.Pro354Ser
|
|
|
NM_006092.2:c.1060C>T
|
NP_006083.1:p.Pro354Ser
|
|
|
XM_005249568.1:c.1060C>T
|
XP_005249625.1:p.Pro354Ser
|
|
|
XM_005249572.1:c.1060C>T
|
XP_005249629.1:p.Pro354Ser
|
|
|
XM_005249576.1:c.316C>T
|
XP_005249633.1:p.Pro106Ser
|
|
|
XM_006715633.2:c.1060C>T
|
XP_006715696.1:p.Pro354Ser
|
|
|
XM_011515079.1:c.1060C>T
|
XP_011513381.1:p.Pro354Ser
|
|
|
XM_011515080.1:c.1060C>T
|
XP_011513382.1:p.Pro354Ser
|
|
|
XM_011515081.1:c.1060C>T
|
XP_011513383.1:p.Pro354Ser
|
|
|
XM_011515082.1:c.1060C>T
|
XP_011513384.1:p.Pro354Ser
|
|
|
XM_011515083.1:c.1060C>T
|
XP_011513385.1:p.Pro354Ser
|
|
|
XM_011515084.1:c.1060C>T
|
XP_011513386.1:p.Pro354Ser
|
|
|
XM_011515085.1:c.1060C>T
|
XP_011513387.1:p.Pro354Ser
|
|
|
XM_011515086.1:c.1060C>T
|
XP_011513388.1:p.Pro354Ser
|
|
|
XM_011515087.1:c.1060C>T
|
XP_011513389.1:p.Pro354Ser
|
|
|
XM_011515088.1:c.1060C>T
|
XP_011513390.1:p.Pro354Ser
|
|
|
XR_926907.1:n.1638C>T
|
|
|
|
XR_926908.1:n.1638C>T
|
|
|
|
XR_926909.1:n.1638C>T
|
|
|
|
XR_926910.1:n.1638C>T
|
|
|
|
NM_001354849.1:c.1060C>T
|
NP_001341778.1:p.Pro354Ser
|
|
|
NM_006092.3:c.1060C>T
|
NP_006083.1:p.Pro354Ser
|
|
|
NR_149002.1:n.1672C>T
|
|
|
|
XM_011515080.2:c.1060C>T
|
XP_011513382.1:p.Pro354Ser
|
|
|
XM_011515081.2:c.1060C>T
|
XP_011513383.1:p.Pro354Ser
|
|
|
XM_011515088.2:c.1060C>T
|
XP_011513390.1:p.Pro354Ser
|
|
|
XM_017011674.1:c.1060C>T
|
XP_016867163.1:p.Pro354Ser
|
|
|
XR_001744529.1:n.1638C>T
|
|
|
|
XR_001744530.1:n.1638C>T
|
|
|
|
XR_002956406.1:n.1586C>T
|
|
|
|
XR_926908.2:n.1638C>T
|
|
|
|
XR_926909.2:n.1638C>T
|
|
|
|
NM_006092.4:c.1060C>T
MANE Select
|
NP_006083.1:p.Pro354Ser
|
|
|
NM_001354849.2:c.1060C>T
|
NP_001341778.1:p.Pro354Ser
|
|
|
NR_149002.2:n.1590C>T
|
|
|
