ENST00000405460.9:c.12122T>A
MANE Select
|
ENSP00000384582.2:p.Val4041Glu
|
|
ENST00000425867.3:c.1076T>A
|
ENSP00000392618.3:p.Val359Glu
|
|
ENST00000639431.1:c.265+87097T>A
|
ENSP00000491057.1:n.265+87097T>A
|
|
ENST00000640464.1:n.2541T>A
|
|
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ENST00000640729.1:n.699T>A
|
|
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ENST00000405460.6:c.12122T>A
|
ENSP00000384582.2:p.Val4041Glu
|
|
NM_032119.3:c.12122T>A
|
NP_115495.3:p.Val4041Glu
|
|
NR_003149.1:n.12135T>A
|
|
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XM_011543675.1:c.12119T>A
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XP_011541977.1:p.Val4040Glu
|
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XM_011543676.1:c.12041T>A
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XP_011541978.1:p.Val4014Glu
|
|
XM_011543677.1:c.9425T>A
|
XP_011541979.1:p.Val3142Glu
|
|
XM_011543678.1:c.12122T>A
|
XP_011541980.1:p.Val4041Glu
|
|
NM_032119.4:c.12122T>A
MANE Select
|
NP_115495.3:p.Val4041Glu
|
|
XM_017009963.2:c.12143T>A
|
XP_016865452.1:p.Val4048Glu
|
|
XM_017009964.2:c.12140T>A
|
XP_016865453.1:p.Val4047Glu
|
|
XM_017009965.1:c.12140T>A
|
XP_016865454.1:p.Val4047Glu
|
|
XM_017009966.2:c.12062T>A
|
XP_016865455.1:p.Val4021Glu
|
|
XM_017009967.1:c.12047T>A
|
XP_016865456.1:p.Val4016Glu
|
|
XM_017009968.2:c.12143T>A
|
XP_016865457.1:p.Val4048Glu
|
|
XM_017009969.2:c.12143T>A
|
XP_016865458.1:p.Val4048Glu
|
|
XM_017009970.2:c.12143T>A
|
XP_016865459.1:p.Val4048Glu
|
|
XM_017009971.2:c.12143T>A
|
XP_016865460.1:p.Val4048Glu
|
|
XM_017009972.1:c.5261T>A
|
XP_016865461.1:p.Val1754Glu
|
|
XM_017009973.1:c.5240T>A
|
XP_016865462.1:p.Val1747Glu
|
|
NR_003149.2:n.12138T>A
|
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