ENST00000255078.8:c.2263A>C
MANE Select
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ENSP00000255078.4:p.Arg755=
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ENST00000674675.1:c.507A>C
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|
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ENST00000674878.1:c.507A>C
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ENST00000674955.1:c.*980A>C
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ENSP00000502463.1:n.*980A>C
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ENST00000675118.1:c.1751A>C
|
|
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ENST00000675389.1:n.538A>C
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|
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ENST00000675615.1:c.2263A>C
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ENSP00000502413.1:p.Arg755=
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ENST00000675648.1:n.1638A>C
|
|
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ENST00000675916.1:c.507A>C
|
|
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ENST00000676173.1:n.3008A>C
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ENST00000676182.1:c.694A>C
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ENST00000676228.1:c.*1586A>C
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ENSP00000502375.1:n.*1586A>C
|
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ENST00000255078.7:c.2263A>C
|
ENSP00000255078.3:p.Arg755=
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ENST00000539064.5:n.2022A>C
|
|
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ENST00000543739.5:n.1256A>C
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NM_002180.2:c.2263A>C , LRG_250t1:c.2263A>C
|
NP_002171.2:p.Arg755=
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XM_005273974.2:c.1252A>C
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XP_005274031.1:p.Arg418=
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XM_005273975.2:c.1135A>C
|
XP_005274032.1:p.Arg379=
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|
XM_011544994.1:c.1030A>C
|
XP_011543296.1:p.Arg344=
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|
XR_949903.1:n.2365A>C
|
|
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XM_005273975.3:c.1135A>C
|
XP_005274032.1:p.Arg379=
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XM_017017669.2:c.1252A>C
|
XP_016873158.1:p.Arg418=
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XM_017017670.2:c.1252A>C
|
XP_016873159.1:p.Arg418=
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|
XR_949903.3:n.2361A>C
|
|
|
NM_002180.3:c.2263A>C
MANE Select
|
NP_002171.2:p.Arg755=
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