ENST00000223051.8:c.785G>C
MANE Select
|
ENSP00000223051.3:p.Arg262Thr
|
|
ENST00000223051.7:c.785G>C
|
ENSP00000223051.3:p.Arg262Thr
|
|
ENST00000431692.5:c.785G>C
|
ENSP00000413905.1:p.Arg262Thr
|
|
ENST00000462090.5:n.26G>C
|
|
|
ENST00000462107.1:c.785G>C
|
ENSP00000420525.1:p.Arg262Thr
|
|
ENST00000465294.5:n.790G>C
|
|
|
ENST00000473374.5:n.235G>C
|
|
|
ENST00000473571.1:n.239G>C
|
|
|
ENST00000475011.1:n.314G>C
|
|
|
ENST00000476304.5:n.406G>C
|
|
|
ENST00000490084.5:c.40G>C
|
|
|
NM_001206855.1:c.272G>C
|
NP_001193784.1:p.Arg91Thr
|
|
NM_003227.3:c.785G>C
|
NP_003218.2:p.Arg262Thr
|
|
XM_005250553.3:c.785G>C
|
XP_005250610.1:p.Arg262Thr
|
|
XM_005250554.3:c.785G>C
|
XP_005250611.1:p.Arg262Thr
|
|
NM_001206855.2:c.272G>C
|
NP_001193784.1:p.Arg91Thr
|
|
XM_005250553.4:c.785G>C
|
XP_005250610.1:p.Arg262Thr
|
|
XM_017012573.1:c.785G>C
|
XP_016868062.1:p.Arg262Thr
|
|
NM_003227.4:c.785G>C
MANE Select
|
NP_003218.2:p.Arg262Thr
|
|
NM_001206855.3:c.272G>C
|
NP_001193784.1:p.Arg91Thr
|
|