ENST00000706989.1:c.2458T>G
|
ENSP00000516702.1:p.Phe820Val
|
|
ENST00000359125.7:c.2404T>G
MANE Select
|
ENSP00000352035.2:p.Phe802Val
|
|
ENST00000637193.1:c.1801T>G
|
ENSP00000490734.1:p.Phe601Val
|
|
ENST00000344462.8:c.2311T>G
|
ENSP00000339611.4:p.Phe771Val
|
|
ENST00000357249.6:c.1972T>G
|
ENSP00000349789.3:p.Phe658Val
|
|
ENST00000359125.6:c.2404T>G
|
ENSP00000352035.2:p.Phe802Val
|
|
ENST00000360480.7:c.2320T>G
|
ENSP00000353668.3:p.Phe774Val
|
|
ENST00000370224.5:c.2241+187T>G
|
ENSP00000359244.2:n.2241+187T>G
|
|
ENST00000625514.2:c.2205+187T>G
|
ENSP00000486040.1:n.2205+187T>G
|
|
ENST00000626839.2:c.2350T>G
|
ENSP00000486706.1:p.Phe784Val
|
|
ENST00000629241.2:c.2133+187T>G
|
ENSP00000487142.1:n.2133+187T>G
|
|
ENST00000629676.2:c.1680-6016T>G
|
ENSP00000486194.1:n.1680-6016T>G
|
|
NM_004518.4:c.2320T>G
|
NP_004509.2:p.Phe774Val
|
|
NM_172106.1:c.2350T>G
|
NP_742104.1:p.Phe784Val
|
|
NM_172107.2:c.2404T>G
|
NP_742105.1:p.Phe802Val
|
|
NM_172108.3:c.2311T>G
|
NP_742106.1:p.Phe771Val
|
|
XM_006723787.1:c.2446T>G
|
XP_006723850.1:p.Phe816Val
|
|
XM_011528807.1:c.2512T>G
|
XP_011527109.1:p.Phe838Val
|
|
XM_011528808.1:c.2509T>G
|
XP_011527110.1:p.Phe837Val
|
|
XM_011528809.1:c.2482T>G
|
XP_011527111.1:p.Phe828Val
|
|
XM_011528810.1:c.2458T>G
|
XP_011527112.1:p.Phe820Val
|
|
XM_011528811.1:c.2428T>G
|
XP_011527113.1:p.Phe810Val
|
|
XM_011528812.1:c.2401T>G
|
XP_011527114.1:p.Phe801Val
|
|
XM_011528813.1:c.2386T>G
|
XP_011527115.1:p.Phe796Val
|
|
XM_011528814.1:c.1993T>G
|
XP_011527116.1:p.Phe665Val
|
|
NM_004518.5:c.2320T>G
|
NP_004509.2:p.Phe774Val
|
|
NM_172106.2:c.2350T>G
|
NP_742104.1:p.Phe784Val
|
|
NM_172107.3:c.2404T>G
|
NP_742105.1:p.Phe802Val
|
|
NM_172108.4:c.2311T>G
|
NP_742106.1:p.Phe771Val
|
|
XM_011528810.2:c.2458T>G
|
XP_011527112.1:p.Phe820Val
|
|
XM_011528811.2:c.2428T>G
|
XP_011527113.1:p.Phe810Val
|
|
XM_017027841.2:c.2455T>G
|
XP_016883330.1:p.Phe819Val
|
|
XM_017027842.2:c.2392T>G
|
XP_016883331.1:p.Phe798Val
|
|
XM_017027843.1:c.2389T>G
|
XP_016883332.1:p.Phe797Val
|
|
XM_017027844.2:c.2347T>G
|
XP_016883333.1:p.Phe783Val
|
|
XM_017027845.1:c.1420T>G
|
XP_016883334.1:p.Phe474Val
|
|
NM_004518.6:c.2320T>G
|
NP_004509.2:p.Phe774Val
|
|
NM_172106.3:c.2350T>G
|
NP_742104.1:p.Phe784Val
|
|
NM_172107.4:c.2404T>G
MANE Select
|
NP_742105.1:p.Phe802Val
|
|
NM_172108.5:c.2311T>G
|
NP_742106.1:p.Phe771Val
|
|
NM_001382235.1:c.2458T>G
|
NP_001369164.1:p.Phe820Val
|
|