ENST00000424310.7:c.608G>C
MANE Select
|
ENSP00000409064.2:p.Arg203Thr
|
|
ENST00000274542.6:c.692G>C
|
ENSP00000274542.2:p.Arg231Thr
|
|
ENST00000424310.6:c.608G>C
|
ENSP00000409064.2:p.Arg203Thr
|
|
ENST00000518802.5:c.698G>C
|
ENSP00000430955.1:p.Arg233Thr
|
|
ENST00000519865.5:c.608G>C
|
ENSP00000430397.1:p.Arg203Thr
|
|
ENST00000520638.1:c.650G>C
|
ENSP00000429071.1:p.Arg217Thr
|
|
ENST00000521606.6:c.659G>C
|
ENSP00000430753.2:p.Arg220Thr
|
|
ENST00000611185.4:c.608G>C
|
ENSP00000482720.1:p.Arg203Thr
|
|
NM_001199380.1:c.698G>C
|
NP_001186309.1:p.Arg233Thr
|
|
NM_001199381.1:c.659G>C
|
NP_001186310.1:p.Arg220Thr
|
|
NM_001199382.1:c.650G>C
|
NP_001186311.1:p.Arg217Thr
|
|
NM_001199383.1:c.608G>C
|
NP_001186312.1:p.Arg203Thr
|
|
NM_144726.2:c.692G>C
|
NP_653327.1:p.Arg231Thr
|
|
XM_005265826.3:c.656G>C
|
XP_005265883.1:p.Arg219Thr
|
|
XM_017009138.2:c.608G>C
|
XP_016864627.1:p.Arg203Thr
|
|
XM_024454383.1:c.656G>C
|
XP_024310151.1:p.Arg219Thr
|
|
NM_001199381.2:c.659G>C
|
NP_001186310.1:p.Arg220Thr
|
|
NM_001199383.2:c.608G>C
MANE Select
|
NP_001186312.1:p.Arg203Thr
|
|
NM_001199380.2:c.698G>C
|
NP_001186309.1:p.Arg233Thr
|
|
NM_001199382.2:c.650G>C
|
NP_001186311.1:p.Arg217Thr
|
|
NM_144726.3:c.692G>C
|
NP_653327.1:p.Arg231Thr
|
|