ENST00000255078.8:c.1974T>C
MANE Select
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ENSP00000255078.4:p.Gly658=
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ENST00000674675.1:c.218T>C
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ENST00000674878.1:c.218T>C
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ENST00000674955.1:c.*691T>C
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ENSP00000502463.1:n.*691T>C
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ENST00000675118.1:c.1462T>C
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|
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ENST00000675389.1:n.249T>C
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ENST00000675615.1:c.1974T>C
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ENSP00000502413.1:p.Gly658=
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ENST00000675648.1:n.1349T>C
|
|
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ENST00000675916.1:c.218T>C
|
|
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ENST00000676173.1:n.2719T>C
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ENST00000676182.1:c.405T>C
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ENST00000676228.1:c.*1297T>C
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ENSP00000502375.1:n.*1297T>C
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ENST00000255078.7:c.1974T>C
|
ENSP00000255078.3:p.Gly658=
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ENST00000539064.5:n.1733T>C
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ENST00000543739.5:n.967T>C
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NM_002180.2:c.1974T>C , LRG_250t1:c.1974T>C
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NP_002171.2:p.Gly658=
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XM_005273974.2:c.963T>C
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XP_005274031.1:p.Gly321=
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XM_005273975.2:c.846T>C
|
XP_005274032.1:p.Gly282=
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XM_011544994.1:c.741T>C
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XP_011543296.1:p.Gly247=
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XR_949903.1:n.2076T>C
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XM_005273975.3:c.846T>C
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XP_005274032.1:p.Gly282=
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XM_017017669.2:c.963T>C
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XP_016873158.1:p.Gly321=
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XM_017017670.2:c.963T>C
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XP_016873159.1:p.Gly321=
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XR_949903.3:n.2072T>C
|
|
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NM_002180.3:c.1974T>C
MANE Select
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NP_002171.2:p.Gly658=
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