|
NM_014875.3:c.2218C>T
MANE Select
|
NP_055690.1:p.Arg740Ter
|
|
ENST00000367350.5:c.2218C>T
MANE Select
|
ENSP00000356319.4:p.Arg740Ter
|
|
NM_001305792.1:c.745C>T
|
NP_001292721.1:p.Arg249Ter
|
|
NM_014875.2:c.2218C>T
|
NP_055690.1:p.Arg740Ter
|
|
ENST00000367350.4:c.2218C>T
|
ENSP00000356319.4:p.Arg740Ter
|
|
ENST00000614960.4:c.2218C>T
|
ENSP00000483069.1:p.Arg740Ter
|
|
XM_011510230.1:c.2218C>T
|
XP_011508532.1:p.Arg740Ter
|
|
XM_011510231.1:c.2218C>T
|
XP_011508533.1:p.Arg740Ter
|
|
XM_011510231.2:c.2218C>T
|
XP_011508533.1:p.Arg740Ter
|
|
XM_011510232.1:c.2218C>T
|
XP_011508534.1:p.Arg740Ter
|
|
XM_011510232.2:c.2218C>T
|
XP_011508534.1:p.Arg740Ter
|
|
XM_011510233.1:c.2134C>T
|
XP_011508535.1:p.Arg712Ter
|
|
XM_011510233.2:c.2134C>T
|
XP_011508535.1:p.Arg712Ter
|
|
XM_011510234.1:c.2119C>T
|
XP_011508536.1:p.Arg707Ter
|
|
XM_011510235.1:c.1846C>T
|
XP_011508537.1:p.Arg616Ter
|
|
XM_011510235.2:c.1846C>T
|
XP_011508537.1:p.Arg616Ter
|
|
XM_011510236.1:c.745C>T
|
XP_011508538.1:p.Arg249Ter
|
|
XM_017003005.1:c.2218C>T
|
XP_016858494.1:p.Arg740Ter
|
|
XM_017003006.1:c.2089C>T
|
XP_016858495.1:p.Arg697Ter
|
|
XM_017003007.1:c.1651C>T
|
XP_016858496.1:p.Arg551Ter
|