ENST00000706989.1:c.2280C>A
|
ENSP00000516702.1:p.Ile760=
|
|
ENST00000359125.7:c.2226C>A
MANE Select
|
ENSP00000352035.2:p.Ile742=
|
|
ENST00000637193.1:c.1623C>A
|
ENSP00000490734.1:p.Ile541=
|
|
ENST00000344462.8:c.2133C>A
|
ENSP00000339611.4:p.Ile711=
|
|
ENST00000357249.6:c.1794C>A
|
ENSP00000349789.3:p.Ile598=
|
|
ENST00000359125.6:c.2226C>A
|
ENSP00000352035.2:p.Ile742=
|
|
ENST00000360480.7:c.2142C>A
|
ENSP00000353668.3:p.Ile714=
|
|
ENST00000370224.5:c.2241+9C>A
|
ENSP00000359244.2:n.2241+9C>A
|
|
ENST00000625514.2:c.2205+9C>A
|
ENSP00000486040.1:n.2205+9C>A
|
|
ENST00000626839.2:c.2172C>A
|
ENSP00000486706.1:p.Ile724=
|
|
ENST00000629241.2:c.2133+9C>A
|
ENSP00000487142.1:n.2133+9C>A
|
|
ENST00000629676.2:c.1680-6194C>A
|
ENSP00000486194.1:n.1680-6194C>A
|
|
NM_004518.4:c.2142C>A
|
NP_004509.2:p.Ile714=
|
|
NM_172106.1:c.2172C>A
|
NP_742104.1:p.Ile724=
|
|
NM_172107.2:c.2226C>A
|
NP_742105.1:p.Ile742=
|
|
NM_172108.3:c.2133C>A
|
NP_742106.1:p.Ile711=
|
|
XM_006723787.1:c.2268C>A
|
XP_006723850.1:p.Ile756=
|
|
XM_011528807.1:c.2334C>A
|
XP_011527109.1:p.Ile778=
|
|
XM_011528808.1:c.2331C>A
|
XP_011527110.1:p.Ile777=
|
|
XM_011528809.1:c.2304C>A
|
XP_011527111.1:p.Ile768=
|
|
XM_011528810.1:c.2280C>A
|
XP_011527112.1:p.Ile760=
|
|
XM_011528811.1:c.2250C>A
|
XP_011527113.1:p.Ile750=
|
|
XM_011528812.1:c.2223C>A
|
XP_011527114.1:p.Ile741=
|
|
XM_011528813.1:c.2208C>A
|
XP_011527115.1:p.Ile736=
|
|
XM_011528814.1:c.1815C>A
|
XP_011527116.1:p.Ile605=
|
|
NM_004518.5:c.2142C>A
|
NP_004509.2:p.Ile714=
|
|
NM_172106.2:c.2172C>A
|
NP_742104.1:p.Ile724=
|
|
NM_172107.3:c.2226C>A
|
NP_742105.1:p.Ile742=
|
|
NM_172108.4:c.2133C>A
|
NP_742106.1:p.Ile711=
|
|
XM_011528810.2:c.2280C>A
|
XP_011527112.1:p.Ile760=
|
|
XM_011528811.2:c.2250C>A
|
XP_011527113.1:p.Ile750=
|
|
XM_017027841.2:c.2277C>A
|
XP_016883330.1:p.Ile759=
|
|
XM_017027842.2:c.2214C>A
|
XP_016883331.1:p.Ile738=
|
|
XM_017027843.1:c.2211C>A
|
XP_016883332.1:p.Ile737=
|
|
XM_017027844.2:c.2169C>A
|
XP_016883333.1:p.Ile723=
|
|
XM_017027845.1:c.1242C>A
|
XP_016883334.1:p.Ile414=
|
|
NM_004518.6:c.2142C>A
|
NP_004509.2:p.Ile714=
|
|
NM_172106.3:c.2172C>A
|
NP_742104.1:p.Ile724=
|
|
NM_172107.4:c.2226C>A
MANE Select
|
NP_742105.1:p.Ile742=
|
|
NM_172108.5:c.2133C>A
|
NP_742106.1:p.Ile711=
|
|
NM_001382235.1:c.2280C>A
|
NP_001369164.1:p.Ile760=
|
|