ENST00000706989.1:c.2378G>T
|
ENSP00000516702.1:p.Arg793Met
|
|
ENST00000359125.7:c.2324G>T
MANE Select
|
ENSP00000352035.2:p.Arg775Met
|
|
ENST00000637193.1:c.1721G>T
|
ENSP00000490734.1:p.Arg574Met
|
|
ENST00000344462.8:c.2231G>T
|
ENSP00000339611.4:p.Arg744Met
|
|
ENST00000357249.6:c.1892G>T
|
ENSP00000349789.3:p.Arg631Met
|
|
ENST00000359125.6:c.2324G>T
|
ENSP00000352035.2:p.Arg775Met
|
|
ENST00000360480.7:c.2240G>T
|
ENSP00000353668.3:p.Arg747Met
|
|
ENST00000370224.5:c.2241+107G>T
|
ENSP00000359244.2:n.2241+107G>T
|
|
ENST00000625514.2:c.2205+107G>T
|
ENSP00000486040.1:n.2205+107G>T
|
|
ENST00000626839.2:c.2270G>T
|
ENSP00000486706.1:p.Arg757Met
|
|
ENST00000629241.2:c.2133+107G>T
|
ENSP00000487142.1:n.2133+107G>T
|
|
ENST00000629676.2:c.1680-6096G>T
|
ENSP00000486194.1:n.1680-6096G>T
|
|
NM_004518.4:c.2240G>T
|
NP_004509.2:p.Arg747Met
|
|
NM_172106.1:c.2270G>T
|
NP_742104.1:p.Arg757Met
|
|
NM_172107.2:c.2324G>T
|
NP_742105.1:p.Arg775Met
|
|
NM_172108.3:c.2231G>T
|
NP_742106.1:p.Arg744Met
|
|
XM_006723787.1:c.2366G>T
|
XP_006723850.1:p.Arg789Met
|
|
XM_011528807.1:c.2432G>T
|
XP_011527109.1:p.Arg811Met
|
|
XM_011528808.1:c.2429G>T
|
XP_011527110.1:p.Arg810Met
|
|
XM_011528809.1:c.2402G>T
|
XP_011527111.1:p.Arg801Met
|
|
XM_011528810.1:c.2378G>T
|
XP_011527112.1:p.Arg793Met
|
|
XM_011528811.1:c.2348G>T
|
XP_011527113.1:p.Arg783Met
|
|
XM_011528812.1:c.2321G>T
|
XP_011527114.1:p.Arg774Met
|
|
XM_011528813.1:c.2306G>T
|
XP_011527115.1:p.Arg769Met
|
|
XM_011528814.1:c.1913G>T
|
XP_011527116.1:p.Arg638Met
|
|
NM_004518.5:c.2240G>T
|
NP_004509.2:p.Arg747Met
|
|
NM_172106.2:c.2270G>T
|
NP_742104.1:p.Arg757Met
|
|
NM_172107.3:c.2324G>T
|
NP_742105.1:p.Arg775Met
|
|
NM_172108.4:c.2231G>T
|
NP_742106.1:p.Arg744Met
|
|
XM_011528810.2:c.2378G>T
|
XP_011527112.1:p.Arg793Met
|
|
XM_011528811.2:c.2348G>T
|
XP_011527113.1:p.Arg783Met
|
|
XM_017027841.2:c.2375G>T
|
XP_016883330.1:p.Arg792Met
|
|
XM_017027842.2:c.2312G>T
|
XP_016883331.1:p.Arg771Met
|
|
XM_017027843.1:c.2309G>T
|
XP_016883332.1:p.Arg770Met
|
|
XM_017027844.2:c.2267G>T
|
XP_016883333.1:p.Arg756Met
|
|
XM_017027845.1:c.1340G>T
|
XP_016883334.1:p.Arg447Met
|
|
NM_004518.6:c.2240G>T
|
NP_004509.2:p.Arg747Met
|
|
NM_172106.3:c.2270G>T
|
NP_742104.1:p.Arg757Met
|
|
NM_172107.4:c.2324G>T
MANE Select
|
NP_742105.1:p.Arg775Met
|
|
NM_172108.5:c.2231G>T
|
NP_742106.1:p.Arg744Met
|
|
NM_001382235.1:c.2378G>T
|
NP_001369164.1:p.Arg793Met
|
|