|
NM_025074.7:c.6433C>T
MANE Select
|
NP_079350.5:p.Arg2145Ter
|
|
ENST00000512123.4:c.6433C>T
MANE Select
|
ENSP00000422834.2:p.Arg2145Ter
|
|
NM_025074.6:c.6433C>T
|
NP_079350.5:p.Arg2145Ter
|
|
ENST00000509802.1:n.418C>T
|
|
|
ENST00000512123.3:c.6433C>T
|
ENSP00000422834.2:p.Arg2145Ter
|
|
ENST00000682513.1:c.6433C>T
|
ENSP00000508201.1:p.Arg2145Ter
|
|
ENST00000684159.1:c.6433C>T
|
ENSP00000506875.1:p.Arg2145Ter
|
|
XM_006714314.1:c.6427C>T
|
XP_006714377.1:p.Arg2143Ter
|
|
XM_006714316.1:c.6433C>T
|
XP_006714379.1:p.Arg2145Ter
|
|
XM_006714316.3:c.6433C>T
|
XP_006714379.1:p.Arg2145Ter
|
|
XM_011532270.1:c.4132C>T
|
XP_011530572.1:p.Arg1378Ter
|
|
XM_011532271.1:c.1321C>T
|
XP_011530573.1:p.Arg441Ter
|