ENST00000512123.4:c.10234C>T
MANE Select
|
ENSP00000422834.2:p.Arg3412Cys
|
|
ENST00000512123.3:c.10234C>T
|
ENSP00000422834.2:p.Arg3412Cys
|
|
NM_025074.6:c.10234C>T
|
NP_079350.5:p.Arg3412Cys
|
|
XM_006714314.1:c.10228C>T
|
XP_006714377.1:p.Arg3410Cys
|
|
XM_006714316.1:c.10006C>T
|
XP_006714379.1:p.Arg3336Cys
|
|
XM_011532270.1:c.7933C>T
|
XP_011530572.1:p.Arg2645Cys
|
|
XM_011532271.1:c.5122C>T
|
XP_011530573.1:p.Arg1708Cys
|
|
XM_006714316.3:c.10006C>T
|
XP_006714379.1:p.Arg3336Cys
|
|
NM_025074.7:c.10234C>T
MANE Select
|
NP_079350.5:p.Arg3412Cys
|
|