ENST00000234071.8:c.801G>C
MANE Select
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ENSP00000234071.4:p.Glu267Asp
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ENST00000234071.7:c.801G>C
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ENSP00000234071.3:p.Glu267Asp
|
|
ENST00000402125.2:c.125G>C
|
|
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ENST00000409048.1:c.903G>C
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ENSP00000386679.1:p.Glu301Asp
|
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NM_000312.3:c.801G>C , LRG_599t1:c.801G>C
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NP_000303.1:p.Glu267Asp
|
|
XM_005263715.3:c.984G>C
|
XP_005263772.1:p.Glu328Asp
|
|
XM_005263716.3:c.966G>C
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XP_005263773.1:p.Glu322Asp
|
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XM_005263717.3:c.864G>C
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XP_005263774.1:p.Glu288Asp
|
|
XR_923313.1:n.1332-97C>G
|
|
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XM_005263717.4:c.864G>C
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XP_005263774.1:p.Glu288Asp
|
|
XM_017004505.1:c.1044G>C
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XP_016859994.1:p.Glu348Asp
|
|
XM_024453002.1:c.1146G>C
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XP_024308770.1:p.Glu382Asp
|
|
XM_024453003.1:c.1086G>C
|
XP_024308771.1:p.Glu362Asp
|
|
XM_024453004.1:c.984G>C
|
XP_024308772.1:p.Glu328Asp
|
|
XM_024453005.1:c.966G>C
|
XP_024308773.1:p.Glu322Asp
|
|
XM_024453006.1:c.903G>C
|
XP_024308774.1:p.Glu301Asp
|
|
XR_001739705.1:n.3607-97C>G
|
|
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XR_923313.2:n.4043-97C>G
|
|
|
NM_000312.4:c.801G>C
MANE Select
|
NP_000303.1:p.Glu267Asp
|
|
NM_001375602.1:c.984G>C
|
NP_001362531.1:p.Glu328Asp
|
|
NM_001375603.1:c.966G>C
|
NP_001362532.1:p.Glu322Asp
|
|
NM_001375604.1:c.864G>C
|
NP_001362533.1:p.Glu288Asp
|
|
NM_001375605.1:c.903G>C
|
NP_001362534.1:p.Glu301Asp
|
|
NM_001375606.1:c.969G>C
|
NP_001362535.1:p.Glu323Asp
|
|
NM_001375607.1:c.987G>C
|
NP_001362536.1:p.Glu329Asp
|
|
NM_001375608.1:c.744G>C
|
NP_001362537.1:p.Glu248Asp
|
|
NM_001375609.1:c.777G>C
|
NP_001362538.1:p.Glu259Asp
|
|
NM_001375610.1:c.795G>C
|
NP_001362539.1:p.Glu265Asp
|
|
NM_001375611.1:c.801G>C
|
NP_001362540.1:p.Glu267Asp
|
|
NM_001375613.1:c.801G>C
|
NP_001362542.1:p.Glu267Asp
|
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