ENST00000532043.2:n.225A>T
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|
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ENST00000682266.1:c.1758A>T
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ENSP00000507766.1:p.Gly586=
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ENST00000682341.1:c.2166A>T
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ENSP00000508251.1:p.Gly722=
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ENST00000683197.1:c.2166A>T
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ENSP00000507641.1:p.Gly722=
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ENST00000683411.1:c.1758A>T
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ENSP00000508397.1:p.Gly586=
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ENST00000683437.1:c.1758A>T
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ENSP00000508408.1:p.Gly586=
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ENST00000683613.1:n.3202A>T
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|
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ENST00000684663.1:c.2163A>T
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ENSP00000508009.1:p.Gly721=
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ENST00000324559.9:c.2208A>T
MANE Select
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ENSP00000315371.9:p.Gly736=
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ENST00000648804.1:n.2543A>T
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|
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ENST00000324559.8:c.2208A>T
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ENSP00000315371.8:p.Gly736=
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ENST00000532043.1:n.225A>T
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|
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NM_001142649.1:c.2205A>T
|
NP_001136121.1:p.Gly735=
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|
NM_213599.2:c.2208A>T , LRG_868t1:c.2208A>T
|
NP_998764.1:p.Gly736=
|
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XM_005252820.2:c.2166A>T
|
XP_005252877.2:p.Gly722=
|
|
XM_005252821.2:c.2163A>T
|
XP_005252878.2:p.Gly721=
|
|
XM_005252822.3:c.2130A>T
|
XP_005252879.1:p.Gly710=
|
|
XM_005252823.3:c.2127A>T
|
XP_005252880.1:p.Gly709=
|
|
XM_011519949.1:c.2115A>T
|
XP_011518251.1:p.Gly705=
|
|
XM_005252820.3:c.2166A>T
|
XP_005252877.2:p.Gly722=
|
|
XM_005252821.3:c.2163A>T
|
XP_005252878.2:p.Gly721=
|
|
XM_005252822.4:c.2130A>T
|
XP_005252879.1:p.Gly710=
|
|
XM_011519949.2:c.2115A>T
|
XP_011518251.1:p.Gly705=
|
|
NM_001142649.2:c.2205A>T
|
NP_001136121.1:p.Gly735=
|
|
NM_213599.3:c.2208A>T
MANE Select
|
NP_998764.1:p.Gly736=
|
|