ENST00000405460.9:c.12135A>C
MANE Select
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ENSP00000384582.2:p.Glu4045Asp
|
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ENST00000425867.3:c.1089A>C
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ENSP00000392618.3:p.Glu363Asp
|
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ENST00000639431.1:c.265+87110A>C
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ENSP00000491057.1:n.265+87110A>C
|
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ENST00000640464.1:n.2554A>C
|
|
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ENST00000640729.1:n.712A>C
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|
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ENST00000405460.6:c.12135A>C
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ENSP00000384582.2:p.Glu4045Asp
|
|
NM_032119.3:c.12135A>C
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NP_115495.3:p.Glu4045Asp
|
|
NR_003149.1:n.12148A>C
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|
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XM_011543675.1:c.12132A>C
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XP_011541977.1:p.Glu4044Asp
|
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XM_011543676.1:c.12054A>C
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XP_011541978.1:p.Glu4018Asp
|
|
XM_011543677.1:c.9438A>C
|
XP_011541979.1:p.Glu3146Asp
|
|
XM_011543678.1:c.12135A>C
|
XP_011541980.1:p.Glu4045Asp
|
|
NM_032119.4:c.12135A>C
MANE Select
|
NP_115495.3:p.Glu4045Asp
|
|
XM_017009963.2:c.12156A>C
|
XP_016865452.1:p.Glu4052Asp
|
|
XM_017009964.2:c.12153A>C
|
XP_016865453.1:p.Glu4051Asp
|
|
XM_017009965.1:c.12153A>C
|
XP_016865454.1:p.Glu4051Asp
|
|
XM_017009966.2:c.12075A>C
|
XP_016865455.1:p.Glu4025Asp
|
|
XM_017009967.1:c.12060A>C
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XP_016865456.1:p.Glu4020Asp
|
|
XM_017009968.2:c.12156A>C
|
XP_016865457.1:p.Glu4052Asp
|
|
XM_017009969.2:c.12156A>C
|
XP_016865458.1:p.Glu4052Asp
|
|
XM_017009970.2:c.12156A>C
|
XP_016865459.1:p.Glu4052Asp
|
|
XM_017009971.2:c.12156A>C
|
XP_016865460.1:p.Glu4052Asp
|
|
XM_017009972.1:c.5274A>C
|
XP_016865461.1:p.Glu1758Asp
|
|
XM_017009973.1:c.5253A>C
|
XP_016865462.1:p.Glu1751Asp
|
|
NR_003149.2:n.12151A>C
|
|
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