ENST00000234071.8:c.1116G>C
MANE Select
|
ENSP00000234071.4:p.Glu372Asp
|
|
ENST00000234071.7:c.1116G>C
|
ENSP00000234071.3:p.Glu372Asp
|
|
ENST00000402125.2:c.440G>C
|
|
|
ENST00000409048.1:c.1218G>C
|
ENSP00000386679.1:p.Glu406Asp
|
|
NM_000312.3:c.1116G>C , LRG_599t1:c.1116G>C
|
NP_000303.1:p.Glu372Asp
|
|
XM_005263715.3:c.1299G>C
|
XP_005263772.1:p.Glu433Asp
|
|
XM_005263716.3:c.1281G>C
|
XP_005263773.1:p.Glu427Asp
|
|
XM_005263717.3:c.1179G>C
|
XP_005263774.1:p.Glu393Asp
|
|
XR_923313.1:n.1332-412C>G
|
|
|
XM_005263717.4:c.1179G>C
|
XP_005263774.1:p.Glu393Asp
|
|
XM_017004505.1:c.1359G>C
|
XP_016859994.1:p.Glu453Asp
|
|
XM_024453002.1:c.1461G>C
|
XP_024308770.1:p.Glu487Asp
|
|
XM_024453003.1:c.1401G>C
|
XP_024308771.1:p.Glu467Asp
|
|
XM_024453004.1:c.1299G>C
|
XP_024308772.1:p.Glu433Asp
|
|
XM_024453005.1:c.1281G>C
|
XP_024308773.1:p.Glu427Asp
|
|
XM_024453006.1:c.1218G>C
|
XP_024308774.1:p.Glu406Asp
|
|
XR_001739705.1:n.3607-412C>G
|
|
|
XR_923313.2:n.4043-412C>G
|
|
|
NM_000312.4:c.1116G>C
MANE Select
|
NP_000303.1:p.Glu372Asp
|
|
NM_001375602.1:c.1299G>C
|
NP_001362531.1:p.Glu433Asp
|
|
NM_001375603.1:c.1281G>C
|
NP_001362532.1:p.Glu427Asp
|
|
NM_001375604.1:c.1179G>C
|
NP_001362533.1:p.Glu393Asp
|
|
NM_001375605.1:c.1218G>C
|
NP_001362534.1:p.Glu406Asp
|
|
NM_001375606.1:c.1284G>C
|
NP_001362535.1:p.Glu428Asp
|
|
NM_001375607.1:c.1302G>C
|
NP_001362536.1:p.Glu434Asp
|
|
NM_001375608.1:c.1059G>C
|
NP_001362537.1:p.Glu353Asp
|
|
NM_001375609.1:c.1092G>C
|
NP_001362538.1:p.Glu364Asp
|
|
NM_001375610.1:c.1110G>C
|
NP_001362539.1:p.Glu370Asp
|
|
NM_001375611.1:c.1116G>C
|
NP_001362540.1:p.Glu372Asp
|
|
NM_001375613.1:c.1116G>C
|
NP_001362542.1:p.Glu372Asp
|
|