ENST00000262494.13:c.616C>T
|
ENSP00000262494.7:p.Arg206Ter
|
|
ENST00000262493.12:c.616C>T
MANE Select
|
ENSP00000262493.6:p.Arg206Ter
|
|
ENST00000262494.12:c.616C>T
|
ENSP00000262494.7:p.Arg206Ter
|
|
ENST00000562316.6:c.283C>T
|
ENSP00000457238.2:p.Arg95Ter
|
|
ENST00000568375.2:c.8C>T
|
|
|
ENST00000638185.1:n.831C>T
|
|
|
ENST00000638210.1:n.916C>T
|
|
|
ENST00000638705.1:c.616C>T
|
ENSP00000491223.1:p.Arg206Ter
|
|
ENST00000638836.1:n.526C>T
|
|
|
ENST00000639055.1:n.1337C>T
|
|
|
ENST00000639251.1:n.517C>T
|
|
|
ENST00000639268.1:c.251C>T
|
|
|
ENST00000639341.1:c.141C>T
|
|
|
ENST00000639770.1:c.654C>T
|
ENSP00000491999.1:n.654C>T
|
|
ENST00000640390.1:n.546C>T
|
|
|
ENST00000640560.1:n.392C>T
|
|
|
ENST00000640893.1:c.*14C>T
|
ENSP00000492677.1:n.*14C>T
|
|
ENST00000262493.10:c.616C>T
|
ENSP00000262493.6:p.Arg206Ter
|
|
ENST00000262494.11:c.616C>T
|
ENSP00000262494.7:p.Arg206Ter
|
|
ENST00000568375.1:n.8C>T
|
|
|
NM_020988.2:c.616C>T
|
NP_066268.1:p.Arg206Ter
|
|
NM_138736.2:c.616C>T
|
NP_620073.2:p.Arg206Ter
|
|
XM_011523003.1:c.490C>T
|
XP_011521305.1:p.Arg164Ter
|
|
XM_011523003.3:c.490C>T
|
XP_011521305.1:p.Arg164Ter
|
|
NM_020988.3:c.616C>T
MANE Select
|
NP_066268.1:p.Arg206Ter
|
|
NM_138736.3:c.616C>T
|
NP_620073.2:p.Arg206Ter
|
|