ENST00000234071.8:c.856T>G
MANE Select
|
ENSP00000234071.4:p.Phe286Val
|
|
ENST00000234071.7:c.856T>G
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ENSP00000234071.3:p.Phe286Val
|
|
ENST00000402125.2:c.180T>G
|
|
|
ENST00000409048.1:c.958T>G
|
ENSP00000386679.1:p.Phe320Val
|
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NM_000312.3:c.856T>G , LRG_599t1:c.856T>G
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NP_000303.1:p.Phe286Val
|
|
XM_005263715.3:c.1039T>G
|
XP_005263772.1:p.Phe347Val
|
|
XM_005263716.3:c.1021T>G
|
XP_005263773.1:p.Phe341Val
|
|
XM_005263717.3:c.919T>G
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XP_005263774.1:p.Phe307Val
|
|
XR_923313.1:n.1332-152A>C
|
|
|
XM_005263717.4:c.919T>G
|
XP_005263774.1:p.Phe307Val
|
|
XM_017004505.1:c.1099T>G
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XP_016859994.1:p.Phe367Val
|
|
XM_024453002.1:c.1201T>G
|
XP_024308770.1:p.Phe401Val
|
|
XM_024453003.1:c.1141T>G
|
XP_024308771.1:p.Phe381Val
|
|
XM_024453004.1:c.1039T>G
|
XP_024308772.1:p.Phe347Val
|
|
XM_024453005.1:c.1021T>G
|
XP_024308773.1:p.Phe341Val
|
|
XM_024453006.1:c.958T>G
|
XP_024308774.1:p.Phe320Val
|
|
XR_001739705.1:n.3607-152A>C
|
|
|
XR_923313.2:n.4043-152A>C
|
|
|
NM_000312.4:c.856T>G
MANE Select
|
NP_000303.1:p.Phe286Val
|
|
NM_001375602.1:c.1039T>G
|
NP_001362531.1:p.Phe347Val
|
|
NM_001375603.1:c.1021T>G
|
NP_001362532.1:p.Phe341Val
|
|
NM_001375604.1:c.919T>G
|
NP_001362533.1:p.Phe307Val
|
|
NM_001375605.1:c.958T>G
|
NP_001362534.1:p.Phe320Val
|
|
NM_001375606.1:c.1024T>G
|
NP_001362535.1:p.Phe342Val
|
|
NM_001375607.1:c.1042T>G
|
NP_001362536.1:p.Phe348Val
|
|
NM_001375608.1:c.799T>G
|
NP_001362537.1:p.Phe267Val
|
|
NM_001375609.1:c.832T>G
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NP_001362538.1:p.Phe278Val
|
|
NM_001375610.1:c.850T>G
|
NP_001362539.1:p.Phe284Val
|
|
NM_001375611.1:c.856T>G
|
NP_001362540.1:p.Phe286Val
|
|
NM_001375613.1:c.856T>G
|
NP_001362542.1:p.Phe286Val
|
|