ENST00000706989.1:c.2424C>G
|
ENSP00000516702.1:p.Ile808Met
|
|
ENST00000359125.7:c.2370C>G
MANE Select
|
ENSP00000352035.2:p.Ile790Met
|
|
ENST00000637193.1:c.1767C>G
|
ENSP00000490734.1:p.Ile589Met
|
|
ENST00000344462.8:c.2277C>G
|
ENSP00000339611.4:p.Ile759Met
|
|
ENST00000357249.6:c.1938C>G
|
ENSP00000349789.3:p.Ile646Met
|
|
ENST00000359125.6:c.2370C>G
|
ENSP00000352035.2:p.Ile790Met
|
|
ENST00000360480.7:c.2286C>G
|
ENSP00000353668.3:p.Ile762Met
|
|
ENST00000370224.5:c.2241+153C>G
|
ENSP00000359244.2:n.2241+153C>G
|
|
ENST00000625514.2:c.2205+153C>G
|
ENSP00000486040.1:n.2205+153C>G
|
|
ENST00000626839.2:c.2316C>G
|
ENSP00000486706.1:p.Ile772Met
|
|
ENST00000629241.2:c.2133+153C>G
|
ENSP00000487142.1:n.2133+153C>G
|
|
ENST00000629676.2:c.1680-6050C>G
|
ENSP00000486194.1:n.1680-6050C>G
|
|
NM_004518.4:c.2286C>G
|
NP_004509.2:p.Ile762Met
|
|
NM_172106.1:c.2316C>G
|
NP_742104.1:p.Ile772Met
|
|
NM_172107.2:c.2370C>G
|
NP_742105.1:p.Ile790Met
|
|
NM_172108.3:c.2277C>G
|
NP_742106.1:p.Ile759Met
|
|
XM_006723787.1:c.2412C>G
|
XP_006723850.1:p.Ile804Met
|
|
XM_011528807.1:c.2478C>G
|
XP_011527109.1:p.Ile826Met
|
|
XM_011528808.1:c.2475C>G
|
XP_011527110.1:p.Ile825Met
|
|
XM_011528809.1:c.2448C>G
|
XP_011527111.1:p.Ile816Met
|
|
XM_011528810.1:c.2424C>G
|
XP_011527112.1:p.Ile808Met
|
|
XM_011528811.1:c.2394C>G
|
XP_011527113.1:p.Ile798Met
|
|
XM_011528812.1:c.2367C>G
|
XP_011527114.1:p.Ile789Met
|
|
XM_011528813.1:c.2352C>G
|
XP_011527115.1:p.Ile784Met
|
|
XM_011528814.1:c.1959C>G
|
XP_011527116.1:p.Ile653Met
|
|
NM_004518.5:c.2286C>G
|
NP_004509.2:p.Ile762Met
|
|
NM_172106.2:c.2316C>G
|
NP_742104.1:p.Ile772Met
|
|
NM_172107.3:c.2370C>G
|
NP_742105.1:p.Ile790Met
|
|
NM_172108.4:c.2277C>G
|
NP_742106.1:p.Ile759Met
|
|
XM_011528810.2:c.2424C>G
|
XP_011527112.1:p.Ile808Met
|
|
XM_011528811.2:c.2394C>G
|
XP_011527113.1:p.Ile798Met
|
|
XM_017027841.2:c.2421C>G
|
XP_016883330.1:p.Ile807Met
|
|
XM_017027842.2:c.2358C>G
|
XP_016883331.1:p.Ile786Met
|
|
XM_017027843.1:c.2355C>G
|
XP_016883332.1:p.Ile785Met
|
|
XM_017027844.2:c.2313C>G
|
XP_016883333.1:p.Ile771Met
|
|
XM_017027845.1:c.1386C>G
|
XP_016883334.1:p.Ile462Met
|
|
NM_004518.6:c.2286C>G
|
NP_004509.2:p.Ile762Met
|
|
NM_172106.3:c.2316C>G
|
NP_742104.1:p.Ile772Met
|
|
NM_172107.4:c.2370C>G
MANE Select
|
NP_742105.1:p.Ile790Met
|
|
NM_172108.5:c.2277C>G
|
NP_742106.1:p.Ile759Met
|
|
NM_001382235.1:c.2424C>G
|
NP_001369164.1:p.Ile808Met
|
|