ENST00000281182.9:c.1155G>T
MANE Select
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ENSP00000281182.5:p.Gln385His
|
|
ENST00000281182.8:c.1155G>T
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ENSP00000281182.4:p.Gln385His
|
|
ENST00000374752.6:c.774G>T
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ENSP00000363884.4:p.Gln258His
|
|
ENST00000524426.5:c.*885G>T
|
ENSP00000431310.1:n.*885G>T
|
|
ENST00000524502.2:n.155G>T
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|
|
ENST00000526026.5:c.*844G>T
|
ENSP00000431532.1:n.*844G>T
|
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ENST00000531338.5:n.1399G>T
|
|
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ENST00000533387.5:n.2214G>T
|
|
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NM_014384.2:c.1155G>T , LRG_448t1:c.1155G>T
|
NP_055199.1:p.Gln385His
|
|
XM_005271501.2:c.1155G>T
|
XP_005271558.1:p.Gln385His
|
|
XM_011542750.1:c.1155G>T
|
XP_011541052.1:p.Gln385His
|
|
XR_947819.1:n.1219G>T
|
|
|
XR_947820.1:n.1607G>T
|
|
|
XR_947821.1:n.1364G>T
|
|
|
XR_947822.1:n.1049G>T
|
|
|
XR_947823.1:n.1205G>T
|
|
|
XM_005271505.4:c.*1420G>T
|
XP_005271562.1:n.*1420G>T
|
|
XM_011542750.3:c.1155G>T
|
XP_011541052.1:p.Gln385His
|
|
XM_017017542.2:c.1155G>T
|
XP_016873031.1:p.Gln385His
|
|
XM_017017543.2:c.1155G>T
|
XP_016873032.1:p.Gln385His
|
|
XM_017017544.2:c.*124G>T
|
XP_016873033.1:n.*124G>T
|
|
XM_017017545.2:c.*367G>T
|
XP_016873034.1:n.*367G>T
|
|
XM_017017546.2:c.861G>T
|
XP_016873035.1:p.Gln287His
|
|
XM_017017547.2:c.861G>T
|
XP_016873036.1:p.Gln287His
|
|
XM_017017548.2:c.*1791G>T
|
XP_016873037.1:n.*1791G>T
|
|
XM_017017549.2:c.*1565G>T
|
XP_016873038.1:n.*1565G>T
|
|
XM_024448437.1:c.*302G>T
|
XP_024304205.1:n.*302G>T
|
|
XM_024448438.1:c.774G>T
|
XP_024304206.1:p.Gln258His
|
|
NM_014384.3:c.1155G>T
MANE Select
|
NP_055199.1:p.Gln385His
|
|