|
NM_025074.7:c.7573C>T
MANE Select
|
NP_079350.5:p.Arg2525Cys
|
|
ENST00000512123.4:c.7573C>T
MANE Select
|
ENSP00000422834.2:p.Arg2525Cys
|
|
NM_025074.6:c.7573C>T
|
NP_079350.5:p.Arg2525Cys
|
|
ENST00000512123.3:c.7573C>T
|
ENSP00000422834.2:p.Arg2525Cys
|
|
ENST00000682513.1:c.7573C>T
|
ENSP00000508201.1:p.Arg2525Cys
|
|
XM_006714314.1:c.7567C>T
|
XP_006714377.1:p.Arg2523Cys
|
|
XM_006714316.1:c.7345C>T
|
XP_006714379.1:p.Arg2449Cys
|
|
XM_006714316.3:c.7345C>T
|
XP_006714379.1:p.Arg2449Cys
|
|
XM_011532270.1:c.5272C>T
|
XP_011530572.1:p.Arg1758Cys
|
|
XM_011532271.1:c.2461C>T
|
XP_011530573.1:p.Arg821Cys
|