ENST00000255078.8:c.2298G>C
MANE Select
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ENSP00000255078.4:p.Gly766=
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ENST00000674675.1:c.542G>C
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ENST00000674878.1:c.542G>C
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ENST00000674955.1:c.*1015G>C
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ENSP00000502463.1:n.*1015G>C
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ENST00000675118.1:c.1786G>C
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|
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ENST00000675389.1:n.573G>C
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ENST00000675615.1:c.2298G>C
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ENSP00000502413.1:p.Gly766=
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ENST00000675648.1:n.1673G>C
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ENST00000675916.1:c.542G>C
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ENST00000676173.1:n.3043G>C
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ENST00000676182.1:c.729G>C
|
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ENST00000676228.1:c.*1621G>C
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ENSP00000502375.1:n.*1621G>C
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ENST00000255078.7:c.2298G>C
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ENSP00000255078.3:p.Gly766=
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ENST00000539064.5:n.2057G>C
|
|
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ENST00000543739.5:n.1291G>C
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NM_002180.2:c.2298G>C , LRG_250t1:c.2298G>C
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NP_002171.2:p.Gly766=
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XM_005273974.2:c.1287G>C
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XP_005274031.1:p.Gly429=
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XM_005273975.2:c.1170G>C
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XP_005274032.1:p.Gly390=
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XM_011544994.1:c.1065G>C
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XP_011543296.1:p.Gly355=
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XR_949903.1:n.2400G>C
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|
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XM_005273975.3:c.1170G>C
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XP_005274032.1:p.Gly390=
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XM_017017669.2:c.1287G>C
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XP_016873158.1:p.Gly429=
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XM_017017670.2:c.1287G>C
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XP_016873159.1:p.Gly429=
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XR_949903.3:n.2396G>C
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NM_002180.3:c.2298G>C
MANE Select
|
NP_002171.2:p.Gly766=
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