ENST00000494137.2:c.671G>C
|
ENSP00000510626.1:p.Arg224Thr
|
|
ENST00000498257.6:c.671G>C
|
ENSP00000510533.1:p.Arg224Thr
|
|
ENST00000617695.5:c.8594G>C
|
ENSP00000481744.2:p.Arg2865Thr
|
|
ENST00000618192.5:c.8870G>C
|
ENSP00000480802.2:p.Arg2957Thr
|
|
ENST00000688198.1:n.1584G>C
|
|
|
ENST00000688799.1:c.671G>C
|
ENSP00000508458.1:p.Arg224Thr
|
|
ENST00000690858.1:n.1600G>C
|
|
|
ENST00000693461.1:n.943G>C
|
|
|
ENST00000421865.3:c.8606G>C
MANE Select
|
ENSP00000400365.2:p.Arg2869Thr
|
|
ENST00000421865.2:c.8606G>C
|
ENSP00000400365.2:p.Arg2869Thr
|
|
ENST00000617695.4:c.8594G>C
|
ENSP00000481744.1:p.Arg2865Thr
|
|
ENST00000618192.4:c.8603G>C
|
ENSP00000480802.1:p.Arg2868Thr
|
|
NM_000426.3:c.8606G>C , LRG_409t1:c.8606G>C
|
NP_000417.2:p.Arg2869Thr
|
|
NM_001079823.1:c.8594G>C
|
NP_001073291.1:p.Arg2865Thr
|
|
XM_005266981.2:c.8870G>C
|
XP_005267038.1:p.Arg2957Thr
|
|
XM_005266982.2:c.8858G>C
|
XP_005267039.1:p.Arg2953Thr
|
|
XM_011535820.1:c.8864G>C
|
XP_011534122.1:p.Arg2955Thr
|
|
XR_942984.1:n.1461-2467C>G
|
|
|
XR_942985.1:n.1325-2467C>G
|
|
|
XM_005266981.3:c.8870G>C
|
XP_005267038.1:p.Arg2957Thr
|
|
XM_005266982.3:c.8858G>C
|
XP_005267039.1:p.Arg2953Thr
|
|
XM_011535820.2:c.8864G>C
|
XP_011534122.1:p.Arg2955Thr
|
|
XM_017010851.2:c.8876G>C
|
XP_016866340.1:p.Arg2959Thr
|
|
XM_017010852.1:c.7001G>C
|
XP_016866341.1:p.Arg2334Thr
|
|
XR_001743859.1:n.3901-2467C>G
|
|
|
XR_001743860.1:n.1180-2467C>G
|
|
|
XR_001743861.1:n.1347-2467C>G
|
|
|
XR_001743863.1:n.883-2467C>G
|
|
|
XR_002956395.1:n.9132-2467C>G
|
|
|
XR_002956396.1:n.3127-2467C>G
|
|
|
NM_000426.4:c.8606G>C
MANE Select
|
NP_000417.3:p.Arg2869Thr
|
|
NM_001079823.2:c.8594G>C
|
NP_001073291.2:p.Arg2865Thr
|
|