ENST00000281182.9:c.1131C>T
MANE Select
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ENSP00000281182.5:p.Gly377=
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|
ENST00000281182.8:c.1131C>T
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ENSP00000281182.4:p.Gly377=
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|
ENST00000374752.6:c.750C>T
|
ENSP00000363884.4:p.Gly250=
|
|
ENST00000524426.5:c.*861C>T
|
ENSP00000431310.1:n.*861C>T
|
|
ENST00000524502.2:n.131C>T
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|
|
ENST00000526026.5:c.*820C>T
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ENSP00000431532.1:n.*820C>T
|
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ENST00000531338.5:n.1375C>T
|
|
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ENST00000533387.5:n.2190C>T
|
|
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NM_014384.2:c.1131C>T , LRG_448t1:c.1131C>T
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NP_055199.1:p.Gly377=
|
|
XM_005271501.2:c.1131C>T
|
XP_005271558.1:p.Gly377=
|
|
XM_011542750.1:c.1131C>T
|
XP_011541052.1:p.Gly377=
|
|
XR_947819.1:n.1195C>T
|
|
|
XR_947820.1:n.1583C>T
|
|
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XR_947821.1:n.1340C>T
|
|
|
XR_947822.1:n.1025C>T
|
|
|
XR_947823.1:n.1181C>T
|
|
|
XM_005271505.4:c.*1396C>T
|
XP_005271562.1:n.*1396C>T
|
|
XM_011542750.3:c.1131C>T
|
XP_011541052.1:p.Gly377=
|
|
XM_017017542.2:c.1131C>T
|
XP_016873031.1:p.Gly377=
|
|
XM_017017543.2:c.1131C>T
|
XP_016873032.1:p.Gly377=
|
|
XM_017017544.2:c.*100C>T
|
XP_016873033.1:n.*100C>T
|
|
XM_017017545.2:c.*343C>T
|
XP_016873034.1:n.*343C>T
|
|
XM_017017546.2:c.837C>T
|
XP_016873035.1:p.Gly279=
|
|
XM_017017547.2:c.837C>T
|
XP_016873036.1:p.Gly279=
|
|
XM_017017548.2:c.*1767C>T
|
XP_016873037.1:n.*1767C>T
|
|
XM_017017549.2:c.*1541C>T
|
XP_016873038.1:n.*1541C>T
|
|
XM_024448437.1:c.*278C>T
|
XP_024304205.1:n.*278C>T
|
|
XM_024448438.1:c.750C>T
|
XP_024304206.1:p.Gly250=
|
|
NM_014384.3:c.1131C>T
MANE Select
|
NP_055199.1:p.Gly377=
|
|