ENST00000405460.9:c.6985G>T
MANE Select
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ENSP00000384582.2:p.Gly2329Ter
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ENST00000639431.1:c.265+16429G>T
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ENSP00000491057.1:n.265+16429G>T
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ENST00000639473.1:n.2444G>T
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ENST00000640012.1:c.792G>T
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ENST00000640374.1:n.129G>T
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ENST00000640403.1:c.4276G>T
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ENSP00000492531.1:p.Gly1426Ter
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ENST00000640779.1:c.1714G>T
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ENST00000405460.6:c.6985G>T
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ENSP00000384582.2:p.Gly2329Ter
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NM_032119.3:c.6985G>T
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NP_115495.3:p.Gly2329Ter
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NR_003149.1:n.6998G>T
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XM_011543675.1:c.6982G>T
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XP_011541977.1:p.Gly2328Ter
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XM_011543676.1:c.6904G>T
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XP_011541978.1:p.Gly2302Ter
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XM_011543677.1:c.4288G>T
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XP_011541979.1:p.Gly1430Ter
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XM_011543678.1:c.6985G>T
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XP_011541980.1:p.Gly2329Ter
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XM_011543679.1:c.6985G>T
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XP_011541981.1:p.Gly2329Ter
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NM_032119.4:c.6985G>T
MANE Select
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NP_115495.3:p.Gly2329Ter
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XM_017009963.2:c.6985G>T
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XP_016865452.1:p.Gly2329Ter
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XM_017009964.2:c.6982G>T
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XP_016865453.1:p.Gly2328Ter
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XM_017009965.1:c.6982G>T
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XP_016865454.1:p.Gly2328Ter
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XM_017009966.2:c.6904G>T
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XP_016865455.1:p.Gly2302Ter
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XM_017009967.1:c.6889G>T
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XP_016865456.1:p.Gly2297Ter
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XM_017009968.2:c.6985G>T
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XP_016865457.1:p.Gly2329Ter
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XM_017009969.2:c.6985G>T
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XP_016865458.1:p.Gly2329Ter
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XM_017009970.2:c.6985G>T
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XP_016865459.1:p.Gly2329Ter
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XM_017009971.2:c.6985G>T
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XP_016865460.1:p.Gly2329Ter
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XM_017009972.1:c.103G>T
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XP_016865461.1:p.Gly35Ter
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XM_017009973.1:c.103G>T
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XP_016865462.1:p.Gly35Ter
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XM_017009974.2:c.6985G>T
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XP_016865463.1:p.Gly2329Ter
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NR_003149.2:n.7001G>T
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