ENST00000706989.1:c.1983C>T
|
ENSP00000516702.1:p.Ile661=
|
|
ENST00000359125.7:c.1929C>T
MANE Select
|
ENSP00000352035.2:p.Ile643=
|
|
ENST00000637193.1:c.1326C>T
|
ENSP00000490734.1:p.Ile442=
|
|
ENST00000637338.1:n.86C>T
|
|
|
ENST00000344462.8:c.1836C>T
|
ENSP00000339611.4:p.Ile612=
|
|
ENST00000357249.6:c.1497C>T
|
ENSP00000349789.3:p.Ile499=
|
|
ENST00000359125.6:c.1929C>T
|
ENSP00000352035.2:p.Ile643=
|
|
ENST00000360480.7:c.1845C>T
|
ENSP00000353668.3:p.Ile615=
|
|
ENST00000370224.5:c.1953C>T
|
ENSP00000359244.2:p.Ile651=
|
|
ENST00000625514.2:c.1917C>T
|
ENSP00000486040.1:p.Ile639=
|
|
ENST00000626839.2:c.1875C>T
|
ENSP00000486706.1:p.Ile625=
|
|
ENST00000629241.2:c.1845C>T
|
ENSP00000487142.1:p.Ile615=
|
|
ENST00000629676.2:c.1679+6116C>T
|
ENSP00000486194.1:n.1679+6116C>T
|
|
NM_004518.4:c.1845C>T
|
NP_004509.2:p.Ile615=
|
|
NM_172106.1:c.1875C>T
|
NP_742104.1:p.Ile625=
|
|
NM_172107.2:c.1929C>T
|
NP_742105.1:p.Ile643=
|
|
NM_172108.3:c.1836C>T
|
NP_742106.1:p.Ile612=
|
|
XM_006723787.1:c.1971C>T
|
XP_006723850.1:p.Ile657=
|
|
XM_011528807.1:c.2037C>T
|
XP_011527109.1:p.Ile679=
|
|
XM_011528808.1:c.2034C>T
|
XP_011527110.1:p.Ile678=
|
|
XM_011528809.1:c.2007C>T
|
XP_011527111.1:p.Ile669=
|
|
XM_011528810.1:c.1983C>T
|
XP_011527112.1:p.Ile661=
|
|
XM_011528811.1:c.1953C>T
|
XP_011527113.1:p.Ile651=
|
|
XM_011528812.1:c.1926C>T
|
XP_011527114.1:p.Ile642=
|
|
XM_011528813.1:c.1911C>T
|
XP_011527115.1:p.Ile637=
|
|
XM_011528814.1:c.1518C>T
|
XP_011527116.1:p.Ile506=
|
|
NM_004518.5:c.1845C>T
|
NP_004509.2:p.Ile615=
|
|
NM_172106.2:c.1875C>T
|
NP_742104.1:p.Ile625=
|
|
NM_172107.3:c.1929C>T
|
NP_742105.1:p.Ile643=
|
|
NM_172108.4:c.1836C>T
|
NP_742106.1:p.Ile612=
|
|
XM_011528810.2:c.1983C>T
|
XP_011527112.1:p.Ile661=
|
|
XM_011528811.2:c.1953C>T
|
XP_011527113.1:p.Ile651=
|
|
XM_017027841.2:c.1980C>T
|
XP_016883330.1:p.Ile660=
|
|
XM_017027842.2:c.1917C>T
|
XP_016883331.1:p.Ile639=
|
|
XM_017027843.1:c.1914C>T
|
XP_016883332.1:p.Ile638=
|
|
XM_017027844.2:c.1872C>T
|
XP_016883333.1:p.Ile624=
|
|
XM_017027845.1:c.945C>T
|
XP_016883334.1:p.Ile315=
|
|
NM_004518.6:c.1845C>T
|
NP_004509.2:p.Ile615=
|
|
NM_172106.3:c.1875C>T
|
NP_742104.1:p.Ile625=
|
|
NM_172107.4:c.1929C>T
MANE Select
|
NP_742105.1:p.Ile643=
|
|
NM_172108.5:c.1836C>T
|
NP_742106.1:p.Ile612=
|
|
NM_001382235.1:c.1983C>T
|
NP_001369164.1:p.Ile661=
|
|