ENST00000405460.9:c.16253T>C
MANE Select
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ENSP00000384582.2:p.Val5418Ala
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ENST00000425867.3:c.5207T>C
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ENSP00000392618.3:p.Val1736Ala
|
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ENST00000638510.1:n.3520T>C
|
|
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ENST00000639431.1:c.265+147272T>C
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ENSP00000491057.1:n.265+147272T>C
|
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ENST00000640061.1:n.128+1299T>C
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|
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ENST00000640407.1:c.2663T>C
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ENSP00000491425.1:p.Val888Ala
|
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ENST00000405460.6:c.16253T>C
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ENSP00000384582.2:p.Val5418Ala
|
|
ENST00000425867.2:c.3236T>C
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ENSP00000392618.2:p.Val1079Ala
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NM_032119.3:c.16253T>C
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NP_115495.3:p.Val5418Ala
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NR_003149.1:n.16266T>C
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|
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XM_011543675.1:c.16250T>C
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XP_011541977.1:p.Val5417Ala
|
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XM_011543676.1:c.16172T>C
|
XP_011541978.1:p.Val5391Ala
|
|
XM_011543677.1:c.13556T>C
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XP_011541979.1:p.Val4519Ala
|
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NM_032119.4:c.16253T>C
MANE Select
|
NP_115495.3:p.Val5418Ala
|
|
XM_017009963.2:c.16274T>C
|
XP_016865452.1:p.Val5425Ala
|
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XM_017009964.2:c.16271T>C
|
XP_016865453.1:p.Val5424Ala
|
|
XM_017009965.1:c.16271T>C
|
XP_016865454.1:p.Val5424Ala
|
|
XM_017009966.2:c.16193T>C
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XP_016865455.1:p.Val5398Ala
|
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XM_017009967.1:c.16178T>C
|
XP_016865456.1:p.Val5393Ala
|
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XM_017009968.2:c.16094T>C
|
XP_016865457.1:p.Val5365Ala
|
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XM_017009969.2:c.16274T>C
|
XP_016865458.1:p.Val5425Ala
|
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XM_017009972.1:c.9392T>C
|
XP_016865461.1:p.Val3131Ala
|
|
XM_017009973.1:c.9371T>C
|
XP_016865462.1:p.Val3124Ala
|
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NR_003149.2:n.16269T>C
|
|
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