ENST00000706989.1:c.2473A>T
|
ENSP00000516702.1:p.Ile825Phe
|
|
ENST00000359125.7:c.2419A>T
MANE Select
|
ENSP00000352035.2:p.Ile807Phe
|
|
ENST00000637193.1:c.1816A>T
|
ENSP00000490734.1:p.Ile606Phe
|
|
ENST00000344462.8:c.2326A>T
|
ENSP00000339611.4:p.Ile776Phe
|
|
ENST00000357249.6:c.1987A>T
|
ENSP00000349789.3:p.Ile663Phe
|
|
ENST00000359125.6:c.2419A>T
|
ENSP00000352035.2:p.Ile807Phe
|
|
ENST00000360480.7:c.2335A>T
|
ENSP00000353668.3:p.Ile779Phe
|
|
ENST00000370224.5:c.2241+202A>T
|
ENSP00000359244.2:n.2241+202A>T
|
|
ENST00000625514.2:c.2205+202A>T
|
ENSP00000486040.1:n.2205+202A>T
|
|
ENST00000626839.2:c.2365A>T
|
ENSP00000486706.1:p.Ile789Phe
|
|
ENST00000629241.2:c.2133+202A>T
|
ENSP00000487142.1:n.2133+202A>T
|
|
ENST00000629676.2:c.1680-6001A>T
|
ENSP00000486194.1:n.1680-6001A>T
|
|
NM_004518.4:c.2335A>T
|
NP_004509.2:p.Ile779Phe
|
|
NM_172106.1:c.2365A>T
|
NP_742104.1:p.Ile789Phe
|
|
NM_172107.2:c.2419A>T
|
NP_742105.1:p.Ile807Phe
|
|
NM_172108.3:c.2326A>T
|
NP_742106.1:p.Ile776Phe
|
|
XM_006723787.1:c.2461A>T
|
XP_006723850.1:p.Ile821Phe
|
|
XM_011528807.1:c.2527A>T
|
XP_011527109.1:p.Ile843Phe
|
|
XM_011528808.1:c.2524A>T
|
XP_011527110.1:p.Ile842Phe
|
|
XM_011528809.1:c.2497A>T
|
XP_011527111.1:p.Ile833Phe
|
|
XM_011528810.1:c.2473A>T
|
XP_011527112.1:p.Ile825Phe
|
|
XM_011528811.1:c.2443A>T
|
XP_011527113.1:p.Ile815Phe
|
|
XM_011528812.1:c.2416A>T
|
XP_011527114.1:p.Ile806Phe
|
|
XM_011528813.1:c.2401A>T
|
XP_011527115.1:p.Ile801Phe
|
|
XM_011528814.1:c.2008A>T
|
XP_011527116.1:p.Ile670Phe
|
|
NM_004518.5:c.2335A>T
|
NP_004509.2:p.Ile779Phe
|
|
NM_172106.2:c.2365A>T
|
NP_742104.1:p.Ile789Phe
|
|
NM_172107.3:c.2419A>T
|
NP_742105.1:p.Ile807Phe
|
|
NM_172108.4:c.2326A>T
|
NP_742106.1:p.Ile776Phe
|
|
XM_011528810.2:c.2473A>T
|
XP_011527112.1:p.Ile825Phe
|
|
XM_011528811.2:c.2443A>T
|
XP_011527113.1:p.Ile815Phe
|
|
XM_017027841.2:c.2470A>T
|
XP_016883330.1:p.Ile824Phe
|
|
XM_017027842.2:c.2407A>T
|
XP_016883331.1:p.Ile803Phe
|
|
XM_017027843.1:c.2404A>T
|
XP_016883332.1:p.Ile802Phe
|
|
XM_017027844.2:c.2362A>T
|
XP_016883333.1:p.Ile788Phe
|
|
XM_017027845.1:c.1435A>T
|
XP_016883334.1:p.Ile479Phe
|
|
NM_004518.6:c.2335A>T
|
NP_004509.2:p.Ile779Phe
|
|
NM_172106.3:c.2365A>T
|
NP_742104.1:p.Ile789Phe
|
|
NM_172107.4:c.2419A>T
MANE Select
|
NP_742105.1:p.Ile807Phe
|
|
NM_172108.5:c.2326A>T
|
NP_742106.1:p.Ile776Phe
|
|
NM_001382235.1:c.2473A>T
|
NP_001369164.1:p.Ile825Phe
|
|