ENST00000264276.11:c.4817T>C
MANE Select
|
ENSP00000264276.6:p.Leu1606Ser
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ENST00000439495.6:c.*997T>C
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ENSP00000403832.2:n.*997T>C
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|
ENST00000679409.1:c.*1287T>C
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ENSP00000506531.1:n.*1287T>C
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|
ENST00000679416.1:n.6321T>C
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|
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ENST00000679427.1:n.2253T>C
|
|
|
ENST00000679435.1:c.4817T>C
|
ENSP00000505218.1:p.Leu1606Ser
|
|
ENST00000679516.1:c.4817T>C
|
ENSP00000505187.1:p.Leu1606Ser
|
|
ENST00000679618.1:c.*1905T>C
|
ENSP00000506274.1:n.*1905T>C
|
|
ENST00000679630.1:n.6666T>C
|
|
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ENST00000679635.1:n.2844T>C
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|
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ENST00000679686.1:n.4931T>C
|
|
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ENST00000679701.1:n.7809T>C
|
|
|
ENST00000679916.1:c.*1165T>C
|
ENSP00000506172.1:n.*1165T>C
|
|
ENST00000680000.1:c.4817T>C
|
ENSP00000506173.1:p.Leu1606Ser
|
|
ENST00000680135.1:c.*2778T>C
|
ENSP00000506211.1:n.*2778T>C
|
|
ENST00000680149.1:c.*99T>C
|
ENSP00000506497.1:n.*99T>C
|
|
ENST00000680163.1:c.4817T>C
|
ENSP00000505092.1:p.Leu1606Ser
|
|
ENST00000680174.1:n.5508T>C
|
|
|
ENST00000680236.1:c.*1878T>C
|
ENSP00000506212.1:n.*1878T>C
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|
ENST00000680404.1:n.332T>C
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|
|
ENST00000680441.1:n.3375T>C
|
|
|
ENST00000680497.1:c.4919T>C
|
ENSP00000505954.1:p.Leu1640Ser
|
|
ENST00000680508.1:c.4814T>C
|
ENSP00000505749.1:p.Leu1605Ser
|
|
ENST00000680569.1:c.*2525T>C
|
ENSP00000505522.1:n.*2525T>C
|
|
ENST00000680634.1:n.1325T>C
|
|
|
ENST00000680722.1:n.2617T>C
|
|
|
ENST00000680726.1:c.*99T>C
|
ENSP00000505505.1:n.*99T>C
|
|
ENST00000680759.1:c.4649T>C
|
ENSP00000505848.1:p.Leu1550Ser
|
|
ENST00000680814.1:c.4817T>C
|
ENSP00000505710.1:p.Leu1606Ser
|
|
ENST00000680828.1:c.*2511T>C
|
ENSP00000505249.1:n.*2511T>C
|
|
ENST00000680861.1:c.4817T>C
|
ENSP00000505043.1:p.Leu1606Ser
|
|
ENST00000680927.1:c.*997T>C
|
ENSP00000505473.1:n.*997T>C
|
|
ENST00000680939.1:n.6523T>C
|
|
|
ENST00000681250.1:c.*1534T>C
|
ENSP00000505684.1:n.*1534T>C
|
|
ENST00000681256.1:c.*2832T>C
|
ENSP00000505446.1:n.*2832T>C
|
|
ENST00000681279.1:n.5683T>C
|
|
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ENST00000681307.1:n.5930T>C
|
|
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ENST00000681461.1:n.5585T>C
|
|
|
ENST00000681495.1:c.2354T>C
|
ENSP00000506085.1:p.Leu785Ser
|
|
ENST00000681558.1:c.2495T>C
|
ENSP00000505568.1:p.Leu832Ser
|
|
ENST00000681619.1:c.4814T>C
|
ENSP00000505071.1:p.Leu1605Ser
|
|
ENST00000681663.1:n.1723T>C
|
|
|
ENST00000681692.1:n.2777T>C
|
|
|
ENST00000681716.1:c.*2671T>C
|
ENSP00000505078.1:n.*2671T>C
|
|
ENST00000681768.1:c.*2481T>C
|
ENSP00000506311.1:n.*2481T>C
|
|
ENST00000681808.1:c.4640T>C
|
ENSP00000505219.1:p.Leu1547Ser
|
|
ENST00000264276.10:c.4817T>C
|
ENSP00000264276.6:p.Leu1606Ser
|
|
ENST00000439495.5:c.2921T>C
|
|
|
NM_020919.3:c.4817T>C
|
NP_065970.2:p.Leu1606Ser
|
|
XM_005246709.2:c.4814T>C
|
XP_005246766.1:p.Leu1605Ser
|
|
XM_006712654.1:c.4817T>C
|
XP_006712717.1:p.Leu1606Ser
|
|
XM_006712655.2:c.2753T>C
|
XP_006712718.1:p.Leu918Ser
|
|
XM_011511530.1:c.4478T>C
|
XP_011509832.1:p.Leu1493Ser
|
|
XR_922974.1:n.5095T>C
|
|
|
XM_006712654.3:c.4817T>C
|
XP_006712717.1:p.Leu1606Ser
|
|
XM_006712655.3:c.2753T>C
|
XP_006712718.1:p.Leu918Ser
|
|
XM_017004569.2:c.4814T>C
|
XP_016860058.1:p.Leu1605Ser
|
|
XM_017004572.2:c.2435T>C
|
XP_016860061.1:p.Leu812Ser
|
|
XM_024453024.1:c.4478T>C
|
XP_024308792.1:p.Leu1493Ser
|
|
XM_024453025.1:c.2750T>C
|
XP_024308793.1:p.Leu917Ser
|
|
XR_001738864.2:n.4932T>C
|
|
|
XR_001738865.2:n.4929T>C
|
|
|
XR_001738866.2:n.5095T>C
|
|
|
XR_001738867.2:n.5092T>C
|
|
|
XR_002959320.1:n.3988T>C
|
|
|
NM_020919.4:c.4817T>C
MANE Select
|
NP_065970.2:p.Leu1606Ser
|
|