|
NM_025074.7:c.11881C>T
MANE Select
|
NP_079350.5:p.Arg3961Trp
|
|
ENST00000512123.4:c.11881C>T
MANE Select
|
ENSP00000422834.2:p.Arg3961Trp
|
|
NM_025074.6:c.11881C>T
|
NP_079350.5:p.Arg3961Trp
|
|
ENST00000512123.3:c.11881C>T
|
ENSP00000422834.2:p.Arg3961Trp
|
|
XM_006714314.1:c.11875C>T
|
XP_006714377.1:p.Arg3959Trp
|
|
XM_006714316.1:c.11653C>T
|
XP_006714379.1:p.Arg3885Trp
|
|
XM_006714316.3:c.11653C>T
|
XP_006714379.1:p.Arg3885Trp
|
|
XM_011532270.1:c.9580C>T
|
XP_011530572.1:p.Arg3194Trp
|
|
XM_011532271.1:c.6769C>T
|
XP_011530573.1:p.Arg2257Trp
|