|
NM_014781.5:c.1702C>T
MANE Select
|
NP_055596.3:p.Arg568Ter
|
|
ENST00000025008.10:c.1702C>T
MANE Select
|
ENSP00000025008.5:p.Arg568Ter
|
|
NM_001083617.1:c.1702C>T
|
NP_001077086.1:p.Arg568Ter
|
|
NM_001083617.2:c.1702C>T
|
NP_001077086.1:p.Arg568Ter
|
|
NM_014781.4:c.1702C>T
|
NP_055596.3:p.Arg568Ter
|
|
ENST00000025008.9:c.1702C>T
|
ENSP00000025008.5:p.Arg568Ter
|
|
ENST00000435644.6:c.1702C>T
|
ENSP00000396067.2:p.Arg568Ter
|
|
ENST00000521611.1:n.385+27982C>T
|
|
|
ENST00000523594.1:c.318C>T
|
|
|
XM_011517643.1:c.1702C>T
|
XP_011515945.1:p.Arg568Ter
|
|
XM_011517643.2:c.1702C>T
|
XP_011515945.1:p.Arg568Ter
|
|
XM_011517644.1:c.1702C>T
|
XP_011515946.1:p.Arg568Ter
|
|
XM_011517644.3:c.1702C>T
|
XP_011515946.1:p.Arg568Ter
|
|
XM_011517645.1:c.1702C>T
|
XP_011515947.1:p.Arg568Ter
|
|
XM_011517645.2:c.1702C>T
|
XP_011515947.1:p.Arg568Ter
|
|
XM_011517646.1:c.1546C>T
|
XP_011515948.1:p.Arg516Ter
|
|
XM_011517646.3:c.1546C>T
|
XP_011515948.1:p.Arg516Ter
|
|
XM_011517647.1:c.1702C>T
|
XP_011515949.1:p.Arg568Ter
|
|
XM_011517647.3:c.1702C>T
|
XP_011515949.1:p.Arg568Ter
|
|
XM_011517648.1:c.1702C>T
|
XP_011515950.1:p.Arg568Ter
|
|
XM_011517649.1:c.1702C>T
|
XP_011515951.1:p.Arg568Ter
|
|
XM_011517649.3:c.1702C>T
|
XP_011515951.1:p.Arg568Ter
|
|
XM_011517650.1:c.73C>T
|
XP_011515952.1:p.Arg25Ter
|
|
XM_017014103.2:c.1702C>T
|
XP_016869592.1:p.Arg568Ter
|
|
XM_017014104.1:c.1702C>T
|
XP_016869593.1:p.Arg568Ter
|
|
XM_017014105.2:c.1702C>T
|
XP_016869594.1:p.Arg568Ter
|
|
XM_017014106.2:c.1702C>T
|
XP_016869595.1:p.Arg568Ter
|
|
XM_017014107.2:c.1702C>T
|
XP_016869596.1:p.Arg568Ter
|
|
XM_017014108.2:c.1702C>T
|
XP_016869597.1:p.Arg568Ter
|
|
XM_017014109.1:c.1546C>T
|
XP_016869598.1:p.Arg516Ter
|
|
XM_017014110.2:c.73C>T
|
XP_016869599.1:p.Arg25Ter
|
|
XM_017014111.2:c.73C>T
|
XP_016869600.1:p.Arg25Ter
|
|
XM_017014112.2:c.73C>T
|
XP_016869601.1:p.Arg25Ter
|
|
XR_928826.1:n.2260C>T
|
|
|
XR_928826.3:n.2250C>T
|
|
