ENST00000255078.8:c.2520G>A
MANE Select
|
ENSP00000255078.4:p.Arg840=
|
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ENST00000674675.1:c.665G>A
|
|
|
ENST00000674878.1:c.625G>A
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|
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ENST00000675118.1:c.2008G>A
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|
|
ENST00000675389.1:n.795G>A
|
|
|
ENST00000675615.1:c.2520G>A
|
ENSP00000502413.1:p.Arg840=
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|
ENST00000675648.1:n.1895G>A
|
|
|
ENST00000675916.1:c.764G>A
|
|
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ENST00000676173.1:n.3265G>A
|
|
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ENST00000676182.1:c.951G>A
|
|
|
ENST00000676228.1:c.*1843G>A
|
ENSP00000502375.1:n.*1843G>A
|
|
ENST00000255078.7:c.2520G>A
|
ENSP00000255078.3:p.Arg840=
|
|
ENST00000539064.5:n.2279G>A
|
|
|
ENST00000543739.5:n.1513G>A
|
|
|
NM_002180.2:c.2520G>A , LRG_250t1:c.2520G>A
|
NP_002171.2:p.Arg840=
|
|
XM_005273974.2:c.1509G>A
|
XP_005274031.1:p.Arg503=
|
|
XM_005273975.2:c.1392G>A
|
XP_005274032.1:p.Arg464=
|
|
XM_011544994.1:c.1287G>A
|
XP_011543296.1:p.Arg429=
|
|
XR_949903.1:n.2622G>A
|
|
|
XM_005273975.3:c.1392G>A
|
XP_005274032.1:p.Arg464=
|
|
XM_017017669.2:c.1509G>A
|
XP_016873158.1:p.Arg503=
|
|
XM_017017670.2:c.1509G>A
|
XP_016873159.1:p.Arg503=
|
|
XR_949903.3:n.2618G>A
|
|
|
NM_002180.3:c.2520G>A
MANE Select
|
NP_002171.2:p.Arg840=
|
|