ENST00000234071.8:c.1209G>C
MANE Select
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ENSP00000234071.4:p.Gly403=
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ENST00000234071.7:c.1209G>C
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ENSP00000234071.3:p.Gly403=
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ENST00000402125.2:c.533G>C
|
|
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ENST00000409048.1:c.1311G>C
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ENSP00000386679.1:p.Gly437=
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NM_000312.3:c.1209G>C , LRG_599t1:c.1209G>C
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NP_000303.1:p.Gly403=
|
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XM_005263715.3:c.1392G>C
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XP_005263772.1:p.Gly464=
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XM_005263716.3:c.1374G>C
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XP_005263773.1:p.Gly458=
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XM_005263717.3:c.1272G>C
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XP_005263774.1:p.Gly424=
|
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XR_923313.1:n.1332-505C>G
|
|
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XM_005263717.4:c.1272G>C
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XP_005263774.1:p.Gly424=
|
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XM_017004505.1:c.1452G>C
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XP_016859994.1:p.Gly484=
|
|
XM_024453002.1:c.1554G>C
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XP_024308770.1:p.Gly518=
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XM_024453003.1:c.1494G>C
|
XP_024308771.1:p.Gly498=
|
|
XM_024453004.1:c.1392G>C
|
XP_024308772.1:p.Gly464=
|
|
XM_024453005.1:c.1374G>C
|
XP_024308773.1:p.Gly458=
|
|
XM_024453006.1:c.1311G>C
|
XP_024308774.1:p.Gly437=
|
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XR_001739705.1:n.3607-505C>G
|
|
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XR_923313.2:n.4043-505C>G
|
|
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NM_000312.4:c.1209G>C
MANE Select
|
NP_000303.1:p.Gly403=
|
|
NM_001375602.1:c.1392G>C
|
NP_001362531.1:p.Gly464=
|
|
NM_001375603.1:c.1374G>C
|
NP_001362532.1:p.Gly458=
|
|
NM_001375604.1:c.1272G>C
|
NP_001362533.1:p.Gly424=
|
|
NM_001375605.1:c.1311G>C
|
NP_001362534.1:p.Gly437=
|
|
NM_001375606.1:c.1377G>C
|
NP_001362535.1:p.Gly459=
|
|
NM_001375607.1:c.1395G>C
|
NP_001362536.1:p.Gly465=
|
|
NM_001375608.1:c.1152G>C
|
NP_001362537.1:p.Gly384=
|
|
NM_001375609.1:c.1185G>C
|
NP_001362538.1:p.Gly395=
|
|
NM_001375610.1:c.1203G>C
|
NP_001362539.1:p.Gly401=
|
|
NM_001375611.1:c.1209G>C
|
NP_001362540.1:p.Gly403=
|
|
NM_001375613.1:c.1209G>C
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NP_001362542.1:p.Gly403=
|
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