ENST00000519811.6:c.1931G>T
MANE Select
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ENSP00000428714.1:p.Gly644Val
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ENST00000262585.6:c.1691G>T
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ENSP00000262585.2:p.Gly564Val
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ENST00000424248.2:c.1535G>T
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ENSP00000410594.1:p.Gly512Val
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ENST00000518668.5:c.1704G>T
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ENST00000519811.5:c.1931G>T
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ENSP00000428714.1:p.Gly644Val
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ENST00000520482.1:n.1472G>T
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NM_014957.2:c.1691G>T
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NP_055772.2:p.Gly564Val
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XM_005250838.3:c.1730G>T
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XP_005250895.2:p.Gly577Val
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XM_005250839.2:c.1730G>T
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XP_005250896.2:p.Gly577Val
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XM_005250840.3:c.1574G>T
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XP_005250897.2:p.Gly525Val
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XM_005250841.2:c.1574G>T
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XP_005250898.2:p.Gly525Val
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XM_005250842.3:c.1697G>T
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XP_005250899.1:p.Gly566Val
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XM_005250843.3:c.1187G>T
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XP_005250900.1:p.Gly396Val
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XM_011516933.1:c.1730G>T
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XP_011515235.1:p.Gly577Val
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XM_011516934.1:c.1730G>T
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XP_011515236.1:p.Gly577Val
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XM_011516935.1:c.1364G>T
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XP_011515237.1:p.Gly455Val
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XM_011516936.1:c.1358G>T
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XP_011515238.1:p.Gly453Val
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XM_011516937.1:c.1730G>T
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XP_011515239.1:p.Gly577Val
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XM_011516938.1:c.899G>T
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XP_011515240.1:p.Gly300Val
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XM_011516939.1:c.428G>T
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XP_011515241.1:p.Gly143Val
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XM_011516940.1:c.428G>T
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XP_011515242.1:p.Gly143Val
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XM_011516941.1:c.1730G>T
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XP_011515243.1:p.Gly577Val
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XM_011516942.1:c.1730G>T
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XP_011515244.1:p.Gly577Val
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XR_242384.2:n.1860G>T
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XR_928310.1:n.1860G>T
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XR_928311.1:n.1860G>T
|
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XR_928312.1:n.1860G>T
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NM_001352890.2:c.1931G>T
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NP_001339819.2:p.Gly644Val
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NM_001362798.1:c.1931G>T
|
NP_001349727.1:p.Gly644Val
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|
NM_014957.4:c.1730G>T
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NP_055772.3:p.Gly577Val
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|
NR_148197.2:n.2027G>T
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XM_005250840.5:c.1775G>T
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XP_005250897.3:p.Gly592Val
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XM_005250841.4:c.1775G>T
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XP_005250898.3:p.Gly592Val
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XM_005250842.4:c.1697G>T
|
XP_005250899.1:p.Gly566Val
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|
XM_011516933.2:c.1931G>T
|
XP_011515235.2:p.Gly644Val
|
|
XM_011516934.3:c.1931G>T
|
XP_011515236.2:p.Gly644Val
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|
XM_011516937.2:c.1931G>T
|
XP_011515239.2:p.Gly644Val
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XM_011516938.3:c.899G>T
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XP_011515240.1:p.Gly300Val
|
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XM_011516939.3:c.428G>T
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XP_011515241.1:p.Gly143Val
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|
XM_011516940.2:c.428G>T
|
XP_011515242.1:p.Gly143Val
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XM_011516941.3:c.1931G>T
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XP_011515243.2:p.Gly644Val
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XM_017013241.1:c.1730G>T
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XP_016868730.1:p.Gly577Val
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|
XM_017013242.1:c.1187G>T
|
XP_016868731.1:p.Gly396Val
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XM_017013243.1:c.467G>T
|
XP_016868732.1:p.Gly156Val
|
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XR_001745497.2:n.2077G>T
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|
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XR_001745498.2:n.2077G>T
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|
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XR_928310.3:n.2077G>T
|
|
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XR_928312.3:n.2077G>T
|
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|
NM_001352890.3:c.1931G>T
MANE Select
|
NP_001339819.2:p.Gly644Val
|
|
NM_001362798.2:c.1931G>T
|
NP_001349727.1:p.Gly644Val
|
|
NM_014957.5:c.1730G>T
|
NP_055772.3:p.Gly577Val
|
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NR_148197.3:n.2050G>T
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