ENST00000234071.8:c.554G>C
MANE Select
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ENSP00000234071.4:p.Arg185Thr
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|
ENST00000234071.7:c.554G>C
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ENSP00000234071.3:p.Arg185Thr
|
|
ENST00000402125.2:c.121-2254G>C
|
|
|
ENST00000409048.1:c.656G>C
|
ENSP00000386679.1:p.Arg219Thr
|
|
ENST00000442644.5:c.497G>C
|
ENSP00000411241.1:p.Arg166Thr
|
|
ENST00000464089.1:n.140G>C
|
|
|
NM_000312.3:c.554G>C , LRG_599t1:c.554G>C
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NP_000303.1:p.Arg185Thr
|
|
XM_005263715.3:c.737G>C
|
XP_005263772.1:p.Arg246Thr
|
|
XM_005263716.3:c.719G>C
|
XP_005263773.1:p.Arg240Thr
|
|
XM_005263717.3:c.617G>C
|
XP_005263774.1:p.Arg206Thr
|
|
XM_005263717.4:c.617G>C
|
XP_005263774.1:p.Arg206Thr
|
|
XM_017004505.1:c.797G>C
|
XP_016859994.1:p.Arg266Thr
|
|
XM_024453002.1:c.899G>C
|
XP_024308770.1:p.Arg300Thr
|
|
XM_024453003.1:c.839G>C
|
XP_024308771.1:p.Arg280Thr
|
|
XM_024453004.1:c.737G>C
|
XP_024308772.1:p.Arg246Thr
|
|
XM_024453005.1:c.719G>C
|
XP_024308773.1:p.Arg240Thr
|
|
XM_024453006.1:c.656G>C
|
XP_024308774.1:p.Arg219Thr
|
|
XR_923313.2:n.4482C>G
|
|
|
NM_000312.4:c.554G>C
MANE Select
|
NP_000303.1:p.Arg185Thr
|
|
NM_001375602.1:c.737G>C
|
NP_001362531.1:p.Arg246Thr
|
|
NM_001375603.1:c.719G>C
|
NP_001362532.1:p.Arg240Thr
|
|
NM_001375604.1:c.617G>C
|
NP_001362533.1:p.Arg206Thr
|
|
NM_001375605.1:c.656G>C
|
NP_001362534.1:p.Arg219Thr
|
|
NM_001375606.1:c.722G>C
|
NP_001362535.1:p.Arg241Thr
|
|
NM_001375607.1:c.740G>C
|
NP_001362536.1:p.Arg247Thr
|
|
NM_001375608.1:c.497G>C
|
NP_001362537.1:p.Arg166Thr
|
|
NM_001375609.1:c.530G>C
|
NP_001362538.1:p.Arg177Thr
|
|
NM_001375610.1:c.548G>C
|
NP_001362539.1:p.Arg183Thr
|
|
NM_001375611.1:c.554G>C
|
NP_001362540.1:p.Arg185Thr
|
|
NM_001375613.1:c.554G>C
|
NP_001362542.1:p.Arg185Thr
|
|