ENST00000700075.1:c.35T>A
|
ENSP00000514784.1:p.Ile12Asn
|
|
ENST00000342771.10:c.1967T>A
MANE Select
|
ENSP00000344087.4:p.Ile656Asn
|
|
ENST00000439256.2:c.65T>A
|
ENSP00000407058.2:p.Ile22Asn
|
|
ENST00000443672.2:c.302T>A
|
ENSP00000393548.2:p.Ile101Asn
|
|
ENST00000449547.6:c.60T>A
|
|
|
ENST00000464768.2:n.635T>A
|
|
|
ENST00000644359.1:c.548T>A
|
ENSP00000494561.1:p.Ile183Asn
|
|
ENST00000644506.1:c.593T>A
|
ENSP00000496672.1:p.Ile198Asn
|
|
ENST00000644939.1:c.1964T>A
|
ENSP00000496726.1:p.Ile655Asn
|
|
ENST00000646136.1:n.278T>A
|
|
|
ENST00000647140.1:c.832T>A
|
|
|
ENST00000342771.8:c.1967T>A
|
ENSP00000344087.4:p.Ile656Asn
|
|
ENST00000406775.6:c.1895T>A
|
ENSP00000385263.2:p.Ile632Asn
|
|
ENST00000439256.1:c.65T>A
|
|
|
ENST00000464768.1:n.633T>A
|
|
|
ENST00000465899.1:n.464T>A
|
|
|
ENST00000498384.5:n.335T>A
|
|
|
ENST00000611706.4:c.1223T>A
|
ENSP00000478134.1:p.Ile408Asn
|
|
ENST00000615871.4:c.1151T>A
|
ENSP00000479325.1:p.Ile384Asn
|
|
NM_001127231.2:c.1895T>A
|
NP_001120703.1:p.Ile632Asn
|
|
NM_015570.3:c.1967T>A
|
NP_056385.1:p.Ile656Asn
|
|
XM_005250257.1:c.614T>A
|
XP_005250314.1:p.Ile205Asn
|
|
XM_011516010.1:c.1988T>A
|
XP_011514312.1:p.Ile663Asn
|
|
XM_011516011.1:c.1985T>A
|
XP_011514313.1:p.Ile662Asn
|
|
XM_011516012.1:c.1922T>A
|
XP_011514314.1:p.Ile641Asn
|
|
XM_011516013.1:c.1916T>A
|
XP_011514315.1:p.Ile639Asn
|
|
XM_011516014.1:c.1886T>A
|
XP_011514316.1:p.Ile629Asn
|
|
XM_011516015.1:c.1724T>A
|
XP_011514317.1:p.Ile575Asn
|
|
XM_011516016.1:c.1697T>A
|
XP_011514318.1:p.Ile566Asn
|
|
XM_011516017.1:c.1514T>A
|
XP_011514319.1:p.Ile505Asn
|
|
XM_011516018.1:c.1487T>A
|
XP_011514320.1:p.Ile496Asn
|
|
XM_005250257.2:c.614T>A
|
XP_005250314.1:p.Ile205Asn
|
|
XM_011516010.2:c.1988T>A
|
XP_011514312.1:p.Ile663Asn
|
|
XM_011516011.2:c.1985T>A
|
XP_011514313.1:p.Ile662Asn
|
|
XM_011516012.2:c.1922T>A
|
XP_011514314.1:p.Ile641Asn
|
|
XM_011516013.2:c.1916T>A
|
XP_011514315.1:p.Ile639Asn
|
|
XM_011516014.2:c.1886T>A
|
XP_011514316.1:p.Ile629Asn
|
|
XM_011516017.2:c.1514T>A
|
XP_011514319.1:p.Ile505Asn
|
|
XM_011516018.2:c.1487T>A
|
XP_011514320.1:p.Ile496Asn
|
|
XM_017011951.2:c.1988T>A
|
XP_016867440.1:p.Ile663Asn
|
|
NM_001127231.3:c.1895T>A
|
NP_001120703.1:p.Ile632Asn
|
|
NM_015570.4:c.1967T>A
MANE Select
|
NP_056385.1:p.Ile656Asn
|
|