ENST00000234071.8:c.914T=
MANE Select
|
ENSP00000234071.4:p.Leu305=
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ENST00000234071.7:c.914T=
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ENSP00000234071.3:p.Leu305=
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ENST00000402125.2:c.238T=
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|
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ENST00000409048.1:c.1016T=
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ENSP00000386679.1:p.Leu339=
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NM_000312.3:c.914T= , LRG_599t1:c.914T=
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NP_000303.1:p.Leu305=
|
|
XM_005263715.3:c.1097T=
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XP_005263772.1:p.Leu366=
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XM_005263716.3:c.1079T=
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XP_005263773.1:p.Leu360=
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XM_005263717.3:c.977T=
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XP_005263774.1:p.Leu326=
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XR_923313.1:n.1332-210A=
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|
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XM_005263717.4:c.977T=
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XP_005263774.1:p.Leu326=
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|
XM_017004505.1:c.1157T=
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XP_016859994.1:p.Leu386=
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|
XM_024453002.1:c.1259T=
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XP_024308770.1:p.Leu420=
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|
XM_024453003.1:c.1199T=
|
XP_024308771.1:p.Leu400=
|
|
XM_024453004.1:c.1097T=
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XP_024308772.1:p.Leu366=
|
|
XM_024453005.1:c.1079T=
|
XP_024308773.1:p.Leu360=
|
|
XM_024453006.1:c.1016T=
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XP_024308774.1:p.Leu339=
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XR_001739705.1:n.3607-210A=
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|
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XR_923313.2:n.4043-210A=
|
|
|
NM_000312.4:c.914T=
MANE Select
|
NP_000303.1:p.Leu305=
|
|
NM_001375602.1:c.1097T=
|
NP_001362531.1:p.Leu366=
|
|
NM_001375603.1:c.1079T=
|
NP_001362532.1:p.Leu360=
|
|
NM_001375604.1:c.977T=
|
NP_001362533.1:p.Leu326=
|
|
NM_001375605.1:c.1016T=
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NP_001362534.1:p.Leu339=
|
|
NM_001375606.1:c.1082T=
|
NP_001362535.1:p.Leu361=
|
|
NM_001375607.1:c.1100T=
|
NP_001362536.1:p.Leu367=
|
|
NM_001375608.1:c.857T=
|
NP_001362537.1:p.Leu286=
|
|
NM_001375609.1:c.890T=
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NP_001362538.1:p.Leu297=
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|
NM_001375610.1:c.908T=
|
NP_001362539.1:p.Leu303=
|
|
NM_001375611.1:c.914T=
|
NP_001362540.1:p.Leu305=
|
|
NM_001375613.1:c.914T=
|
NP_001362542.1:p.Leu305=
|
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