ENST00000706989.1:c.2353C>T
|
ENSP00000516702.1:p.Arg785Trp
|
|
ENST00000359125.7:c.2299C>T
MANE Select
|
ENSP00000352035.2:p.Arg767Trp
|
|
ENST00000637193.1:c.1696C>T
|
ENSP00000490734.1:p.Arg566Trp
|
|
ENST00000344462.8:c.2206C>T
|
ENSP00000339611.4:p.Arg736Trp
|
|
ENST00000357249.6:c.1867C>T
|
ENSP00000349789.3:p.Arg623Trp
|
|
ENST00000359125.6:c.2299C>T
|
ENSP00000352035.2:p.Arg767Trp
|
|
ENST00000360480.7:c.2215C>T
|
ENSP00000353668.3:p.Arg739Trp
|
|
ENST00000370224.5:c.2241+82C>T
|
ENSP00000359244.2:n.2241+82C>T
|
|
ENST00000625514.2:c.2205+82C>T
|
ENSP00000486040.1:n.2205+82C>T
|
|
ENST00000626839.2:c.2245C>T
|
ENSP00000486706.1:p.Arg749Trp
|
|
ENST00000629241.2:c.2133+82C>T
|
ENSP00000487142.1:n.2133+82C>T
|
|
ENST00000629676.2:c.1680-6121C>T
|
ENSP00000486194.1:n.1680-6121C>T
|
|
NM_004518.4:c.2215C>T
|
NP_004509.2:p.Arg739Trp
|
|
NM_172106.1:c.2245C>T
|
NP_742104.1:p.Arg749Trp
|
|
NM_172107.2:c.2299C>T
|
NP_742105.1:p.Arg767Trp
|
|
NM_172108.3:c.2206C>T
|
NP_742106.1:p.Arg736Trp
|
|
XM_006723787.1:c.2341C>T
|
XP_006723850.1:p.Arg781Trp
|
|
XM_011528807.1:c.2407C>T
|
XP_011527109.1:p.Arg803Trp
|
|
XM_011528808.1:c.2404C>T
|
XP_011527110.1:p.Arg802Trp
|
|
XM_011528809.1:c.2377C>T
|
XP_011527111.1:p.Arg793Trp
|
|
XM_011528810.1:c.2353C>T
|
XP_011527112.1:p.Arg785Trp
|
|
XM_011528811.1:c.2323C>T
|
XP_011527113.1:p.Arg775Trp
|
|
XM_011528812.1:c.2296C>T
|
XP_011527114.1:p.Arg766Trp
|
|
XM_011528813.1:c.2281C>T
|
XP_011527115.1:p.Arg761Trp
|
|
XM_011528814.1:c.1888C>T
|
XP_011527116.1:p.Arg630Trp
|
|
NM_004518.5:c.2215C>T
|
NP_004509.2:p.Arg739Trp
|
|
NM_172106.2:c.2245C>T
|
NP_742104.1:p.Arg749Trp
|
|
NM_172107.3:c.2299C>T
|
NP_742105.1:p.Arg767Trp
|
|
NM_172108.4:c.2206C>T
|
NP_742106.1:p.Arg736Trp
|
|
XM_011528810.2:c.2353C>T
|
XP_011527112.1:p.Arg785Trp
|
|
XM_011528811.2:c.2323C>T
|
XP_011527113.1:p.Arg775Trp
|
|
XM_017027841.2:c.2350C>T
|
XP_016883330.1:p.Arg784Trp
|
|
XM_017027842.2:c.2287C>T
|
XP_016883331.1:p.Arg763Trp
|
|
XM_017027843.1:c.2284C>T
|
XP_016883332.1:p.Arg762Trp
|
|
XM_017027844.2:c.2242C>T
|
XP_016883333.1:p.Arg748Trp
|
|
XM_017027845.1:c.1315C>T
|
XP_016883334.1:p.Arg439Trp
|
|
NM_004518.6:c.2215C>T
|
NP_004509.2:p.Arg739Trp
|
|
NM_172106.3:c.2245C>T
|
NP_742104.1:p.Arg749Trp
|
|
NM_172107.4:c.2299C>T
MANE Select
|
NP_742105.1:p.Arg767Trp
|
|
NM_172108.5:c.2206C>T
|
NP_742106.1:p.Arg736Trp
|
|
NM_001382235.1:c.2353C>T
|
NP_001369164.1:p.Arg785Trp
|
|