|
ENST00000400017.7:c.2043G>T
MANE Select
|
ENSP00000382895.2:p.Gln681His
|
|
|
ENST00000382933.8:c.689-2725G>T
|
ENSP00000372391.4:n.689-2725G>T
|
|
|
ENST00000400017.6:c.2043G>T
|
ENSP00000382895.2:p.Gln681His
|
|
|
ENST00000553500.5:n.328+173G>T
|
|
|
|
ENST00000553927.1:n.975G>T
|
|
|
|
ENST00000554303.1:c.429G>T
|
ENSP00000450426.1:p.Gln143His
|
|
|
ENST00000555322.5:c.470G>T
|
|
|
|
ENST00000555489.5:c.236G>T
|
ENSP00000451044.1:n.236G>T
|
|
|
ENST00000555587.5:c.468G>T
|
ENSP00000451262.1:p.Gln156His
|
|
|
ENST00000556336.5:c.1682-2725G>T
|
ENSP00000450445.1:n.1682-2725G>T
|
|
|
ENST00000557771.5:c.1929G>T
|
ENSP00000451219.1:p.Gln643His
|
|
|
NM_020366.3:c.2043G>T
|
NP_065099.3:p.Gln681His
|
|
|
XM_005267879.2:c.969G>T
|
XP_005267936.1:p.Gln323His
|
|
|
XM_005267880.2:c.936G>T
|
XP_005267937.1:p.Gln312His
|
|
|
XM_005267881.2:c.417G>T
|
XP_005267938.1:p.Gln139His
|
|
|
XM_011536978.1:c.969G>T
|
XP_011535280.1:p.Gln323His
|
|
|
XM_011536979.1:c.797-44G>T
|
XP_011535281.1:n.797-44G>T
|
|
|
XM_011536980.1:c.796+173G>T
|
XP_011535282.1:n.796+173G>T
|
|
|
XM_011536981.1:c.969G>T
|
XP_011535283.1:p.Gln323His
|
|
|
XM_011536982.1:c.796+173G>T
|
XP_011535284.1:n.796+173G>T
|
|
|
XM_011536983.1:c.2010G>T
|
XP_011535285.1:p.Gln670His
|
|
|
XM_005267881.3:c.417G>T
|
XP_005267938.1:p.Gln139His
|
|
|
XM_017021473.1:c.969G>T
|
XP_016876962.1:p.Gln323His
|
|
|
XM_024449663.1:c.969G>T
|
XP_024305431.1:p.Gln323His
|
|
|
XM_024449664.1:c.969G>T
|
XP_024305432.1:p.Gln323His
|
|
|
XM_024449665.1:c.796+173G>T
|
XP_024305433.1:n.796+173G>T
|
|
|
XM_024449666.1:c.796+173G>T
|
XP_024305434.1:n.796+173G>T
|
|
|
NM_001377523.1:c.689-2725G>T
|
NP_001364452.1:n.689-2725G>T
|
|
|
NM_001377948.1:c.969G>T
|
NP_001364877.1:p.Gln323His
|
|
|
NM_001377949.1:c.796+173G>T
|
NP_001364878.1:n.796+173G>T
|
|
|
NM_001377950.1:c.689-2725G>T
|
NP_001364879.1:n.689-2725G>T
|
|
|
NM_001377951.1:c.191-2725G>T
|
NP_001364880.1:n.191-2725G>T
|
|
|
NM_020366.4:c.2043G>T
MANE Select
|
NP_065099.3:p.Gln681His
|
|
