ENST00000519811.6:c.2257T>G
MANE Select
|
ENSP00000428714.1:p.Phe753Val
|
|
ENST00000262585.6:c.2017T>G
|
ENSP00000262585.2:p.Phe673Val
|
|
ENST00000424248.2:c.1861T>G
|
ENSP00000410594.1:p.Phe621Val
|
|
ENST00000518668.5:c.2030T>G
|
|
|
ENST00000519811.5:c.2257T>G
|
ENSP00000428714.1:p.Phe753Val
|
|
ENST00000520482.1:n.1798T>G
|
|
|
NM_014957.2:c.2017T>G
|
NP_055772.2:p.Phe673Val
|
|
XM_005250838.3:c.2056T>G
|
XP_005250895.2:p.Phe686Val
|
|
XM_005250839.2:c.2056T>G
|
XP_005250896.2:p.Phe686Val
|
|
XM_005250840.3:c.1900T>G
|
XP_005250897.2:p.Phe634Val
|
|
XM_005250841.2:c.1900T>G
|
XP_005250898.2:p.Phe634Val
|
|
XM_005250842.3:c.2023T>G
|
XP_005250899.1:p.Phe675Val
|
|
XM_005250843.3:c.1513T>G
|
XP_005250900.1:p.Phe505Val
|
|
XM_011516933.1:c.2056T>G
|
XP_011515235.1:p.Phe686Val
|
|
XM_011516934.1:c.2056T>G
|
XP_011515236.1:p.Phe686Val
|
|
XM_011516935.1:c.1690T>G
|
XP_011515237.1:p.Phe564Val
|
|
XM_011516936.1:c.1684T>G
|
XP_011515238.1:p.Phe562Val
|
|
XM_011516937.1:c.2056T>G
|
XP_011515239.1:p.Phe686Val
|
|
XM_011516938.1:c.1225T>G
|
XP_011515240.1:p.Phe409Val
|
|
XM_011516939.1:c.754T>G
|
XP_011515241.1:p.Phe252Val
|
|
XM_011516940.1:c.754T>G
|
XP_011515242.1:p.Phe252Val
|
|
XM_011516941.1:c.2056T>G
|
XP_011515243.1:p.Phe686Val
|
|
XM_011516942.1:c.2056T>G
|
XP_011515244.1:p.Phe686Val
|
|
XR_242384.2:n.2186T>G
|
|
|
XR_928310.1:n.2186T>G
|
|
|
XR_928311.1:n.2186T>G
|
|
|
XR_928312.1:n.2186T>G
|
|
|
NM_001352890.2:c.2257T>G
|
NP_001339819.2:p.Phe753Val
|
|
NM_001362798.1:c.2257T>G
|
NP_001349727.1:p.Phe753Val
|
|
NM_014957.4:c.2056T>G
|
NP_055772.3:p.Phe686Val
|
|
NR_148197.2:n.2353T>G
|
|
|
XM_005250840.5:c.2101T>G
|
XP_005250897.3:p.Phe701Val
|
|
XM_005250841.4:c.2101T>G
|
XP_005250898.3:p.Phe701Val
|
|
XM_005250842.4:c.2023T>G
|
XP_005250899.1:p.Phe675Val
|
|
XM_011516933.2:c.2257T>G
|
XP_011515235.2:p.Phe753Val
|
|
XM_011516934.3:c.2257T>G
|
XP_011515236.2:p.Phe753Val
|
|
XM_011516937.2:c.2257T>G
|
XP_011515239.2:p.Phe753Val
|
|
XM_011516938.3:c.1225T>G
|
XP_011515240.1:p.Phe409Val
|
|
XM_011516939.3:c.754T>G
|
XP_011515241.1:p.Phe252Val
|
|
XM_011516940.2:c.754T>G
|
XP_011515242.1:p.Phe252Val
|
|
XM_011516941.3:c.2257T>G
|
XP_011515243.2:p.Phe753Val
|
|
XM_017013241.1:c.2056T>G
|
XP_016868730.1:p.Phe686Val
|
|
XM_017013242.1:c.1513T>G
|
XP_016868731.1:p.Phe505Val
|
|
XM_017013243.1:c.793T>G
|
XP_016868732.1:p.Phe265Val
|
|
XR_001745497.2:n.2403T>G
|
|
|
XR_001745498.2:n.2403T>G
|
|
|
XR_928310.3:n.2403T>G
|
|
|
XR_928312.3:n.2403T>G
|
|
|
NM_001352890.3:c.2257T>G
MANE Select
|
NP_001339819.2:p.Phe753Val
|
|
NM_001362798.2:c.2257T>G
|
NP_001349727.1:p.Phe753Val
|
|
NM_014957.5:c.2056T>G
|
NP_055772.3:p.Phe686Val
|
|
NR_148197.3:n.2376T>G
|
|
|