ENST00000405460.9:c.7063G>T
MANE Select
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ENSP00000384582.2:p.Ala2355Ser
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ENST00000639431.1:c.265+16507G>T
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ENSP00000491057.1:n.265+16507G>T
|
|
ENST00000639473.1:n.2522G>T
|
|
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ENST00000640012.1:c.870G>T
|
|
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ENST00000640374.1:n.207G>T
|
|
|
ENST00000640403.1:c.4354G>T
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ENSP00000492531.1:p.Ala1452Ser
|
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ENST00000640779.1:c.1792G>T
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|
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ENST00000405460.6:c.7063G>T
|
ENSP00000384582.2:p.Ala2355Ser
|
|
NM_032119.3:c.7063G>T
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NP_115495.3:p.Ala2355Ser
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NR_003149.1:n.7076G>T
|
|
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XM_011543675.1:c.7060G>T
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XP_011541977.1:p.Ala2354Ser
|
|
XM_011543676.1:c.6982G>T
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XP_011541978.1:p.Ala2328Ser
|
|
XM_011543677.1:c.4366G>T
|
XP_011541979.1:p.Ala1456Ser
|
|
XM_011543678.1:c.7063G>T
|
XP_011541980.1:p.Ala2355Ser
|
|
XM_011543679.1:c.7063G>T
|
XP_011541981.1:p.Ala2355Ser
|
|
NM_032119.4:c.7063G>T
MANE Select
|
NP_115495.3:p.Ala2355Ser
|
|
XM_017009963.2:c.7063G>T
|
XP_016865452.1:p.Ala2355Ser
|
|
XM_017009964.2:c.7060G>T
|
XP_016865453.1:p.Ala2354Ser
|
|
XM_017009965.1:c.7060G>T
|
XP_016865454.1:p.Ala2354Ser
|
|
XM_017009966.2:c.6982G>T
|
XP_016865455.1:p.Ala2328Ser
|
|
XM_017009967.1:c.6967G>T
|
XP_016865456.1:p.Ala2323Ser
|
|
XM_017009968.2:c.7063G>T
|
XP_016865457.1:p.Ala2355Ser
|
|
XM_017009969.2:c.7063G>T
|
XP_016865458.1:p.Ala2355Ser
|
|
XM_017009970.2:c.7063G>T
|
XP_016865459.1:p.Ala2355Ser
|
|
XM_017009971.2:c.7063G>T
|
XP_016865460.1:p.Ala2355Ser
|
|
XM_017009972.1:c.181G>T
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XP_016865461.1:p.Ala61Ser
|
|
XM_017009973.1:c.181G>T
|
XP_016865462.1:p.Ala61Ser
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|
XM_017009974.2:c.7063G>T
|
XP_016865463.1:p.Ala2355Ser
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NR_003149.2:n.7079G>T
|
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