ENST00000405460.9:c.9433G>T
MANE Select
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ENSP00000384582.2:p.Gly3145Cys
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ENST00000639431.1:c.265+40506G>T
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ENSP00000491057.1:n.265+40506G>T
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ENST00000639473.1:n.4892G>T
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|
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ENST00000640012.1:c.3240G>T
|
|
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ENST00000640374.1:n.2577G>T
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|
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ENST00000640779.1:c.4162G>T
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|
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ENST00000405460.6:c.9433G>T
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ENSP00000384582.2:p.Gly3145Cys
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ENST00000509621.1:c.2130G>T
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NM_032119.3:c.9433G>T
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NP_115495.3:p.Gly3145Cys
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NR_003149.1:n.9446G>T
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|
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XM_011543675.1:c.9430G>T
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XP_011541977.1:p.Gly3144Cys
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XM_011543676.1:c.9352G>T
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XP_011541978.1:p.Gly3118Cys
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XM_011543677.1:c.6736G>T
|
XP_011541979.1:p.Gly2246Cys
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XM_011543678.1:c.9433G>T
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XP_011541980.1:p.Gly3145Cys
|
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XM_011543679.1:c.9433G>T
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XP_011541981.1:p.Gly3145Cys
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XR_948560.1:n.272-906C>A
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|
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NM_032119.4:c.9433G>T
MANE Select
|
NP_115495.3:p.Gly3145Cys
|
|
XM_017009963.2:c.9454G>T
|
XP_016865452.1:p.Gly3152Cys
|
|
XM_017009964.2:c.9451G>T
|
XP_016865453.1:p.Gly3151Cys
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XM_017009965.1:c.9451G>T
|
XP_016865454.1:p.Gly3151Cys
|
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XM_017009966.2:c.9373G>T
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XP_016865455.1:p.Gly3125Cys
|
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XM_017009967.1:c.9358G>T
|
XP_016865456.1:p.Gly3120Cys
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XM_017009968.2:c.9454G>T
|
XP_016865457.1:p.Gly3152Cys
|
|
XM_017009969.2:c.9454G>T
|
XP_016865458.1:p.Gly3152Cys
|
|
XM_017009970.2:c.9454G>T
|
XP_016865459.1:p.Gly3152Cys
|
|
XM_017009971.2:c.9454G>T
|
XP_016865460.1:p.Gly3152Cys
|
|
XM_017009972.1:c.2572G>T
|
XP_016865461.1:p.Gly858Cys
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XM_017009973.1:c.2551G>T
|
XP_016865462.1:p.Gly851Cys
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|
XM_017009974.2:c.9454G>T
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XP_016865463.1:p.Gly3152Cys
|
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XR_001742802.1:n.2523-906C>A
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NR_003149.2:n.9449G>T
|
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