ENST00000234071.8:c.666C>G
MANE Select
|
ENSP00000234071.4:p.Asp222Glu
|
|
ENST00000234071.7:c.666C>G
|
ENSP00000234071.3:p.Asp222Glu
|
|
ENST00000402125.2:c.121-2142C>G
|
|
|
ENST00000409048.1:c.768C>G
|
ENSP00000386679.1:p.Asp256Glu
|
|
ENST00000464089.1:n.252C>G
|
|
|
NM_000312.3:c.666C>G , LRG_599t1:c.666C>G
|
NP_000303.1:p.Asp222Glu
|
|
XM_005263715.3:c.849C>G
|
XP_005263772.1:p.Asp283Glu
|
|
XM_005263716.3:c.831C>G
|
XP_005263773.1:p.Asp277Glu
|
|
XM_005263717.3:c.729C>G
|
XP_005263774.1:p.Asp243Glu
|
|
XM_005263717.4:c.729C>G
|
XP_005263774.1:p.Asp243Glu
|
|
XM_017004505.1:c.909C>G
|
XP_016859994.1:p.Asp303Glu
|
|
XM_024453002.1:c.1011C>G
|
XP_024308770.1:p.Asp337Glu
|
|
XM_024453003.1:c.951C>G
|
XP_024308771.1:p.Asp317Glu
|
|
XM_024453004.1:c.849C>G
|
XP_024308772.1:p.Asp283Glu
|
|
XM_024453005.1:c.831C>G
|
XP_024308773.1:p.Asp277Glu
|
|
XM_024453006.1:c.768C>G
|
XP_024308774.1:p.Asp256Glu
|
|
XR_923313.2:n.4370G>C
|
|
|
NM_000312.4:c.666C>G
MANE Select
|
NP_000303.1:p.Asp222Glu
|
|
NM_001375602.1:c.849C>G
|
NP_001362531.1:p.Asp283Glu
|
|
NM_001375603.1:c.831C>G
|
NP_001362532.1:p.Asp277Glu
|
|
NM_001375604.1:c.729C>G
|
NP_001362533.1:p.Asp243Glu
|
|
NM_001375605.1:c.768C>G
|
NP_001362534.1:p.Asp256Glu
|
|
NM_001375606.1:c.834C>G
|
NP_001362535.1:p.Asp278Glu
|
|
NM_001375607.1:c.852C>G
|
NP_001362536.1:p.Asp284Glu
|
|
NM_001375608.1:c.609C>G
|
NP_001362537.1:p.Asp203Glu
|
|
NM_001375609.1:c.642C>G
|
NP_001362538.1:p.Asp214Glu
|
|
NM_001375610.1:c.660C>G
|
NP_001362539.1:p.Asp220Glu
|
|
NM_001375611.1:c.666C>G
|
NP_001362540.1:p.Asp222Glu
|
|
NM_001375613.1:c.666C>G
|
NP_001362542.1:p.Asp222Glu
|
|