|
ENST00000400017.7:c.2012G>T
MANE Select
|
ENSP00000382895.2:p.Gly671Val
|
|
|
ENST00000382933.8:c.689-2756G>T
|
ENSP00000372391.4:n.689-2756G>T
|
|
|
ENST00000400017.6:c.2012G>T
|
ENSP00000382895.2:p.Gly671Val
|
|
|
ENST00000553500.5:n.328+142G>T
|
|
|
|
ENST00000553927.1:n.944G>T
|
|
|
|
ENST00000554303.1:c.398G>T
|
ENSP00000450426.1:p.Gly133Val
|
|
|
ENST00000555322.5:c.439G>T
|
|
|
|
ENST00000555489.5:c.213-8G>T
|
ENSP00000451044.1:n.213-8G>T
|
|
|
ENST00000555587.5:c.437G>T
|
ENSP00000451262.1:p.Gly146Val
|
|
|
ENST00000556336.5:c.1682-2756G>T
|
ENSP00000450445.1:n.1682-2756G>T
|
|
|
ENST00000557771.5:c.1898G>T
|
ENSP00000451219.1:p.Gly633Val
|
|
|
NM_020366.3:c.2012G>T
|
NP_065099.3:p.Gly671Val
|
|
|
XM_005267879.2:c.938G>T
|
XP_005267936.1:p.Gly313Val
|
|
|
XM_005267880.2:c.905G>T
|
XP_005267937.1:p.Gly302Val
|
|
|
XM_005267881.2:c.386G>T
|
XP_005267938.1:p.Gly129Val
|
|
|
XM_011536978.1:c.938G>T
|
XP_011535280.1:p.Gly313Val
|
|
|
XM_011536979.1:c.797-75G>T
|
XP_011535281.1:n.797-75G>T
|
|
|
XM_011536980.1:c.796+142G>T
|
XP_011535282.1:n.796+142G>T
|
|
|
XM_011536981.1:c.938G>T
|
XP_011535283.1:p.Gly313Val
|
|
|
XM_011536982.1:c.796+142G>T
|
XP_011535284.1:n.796+142G>T
|
|
|
XM_011536983.1:c.1979G>T
|
XP_011535285.1:p.Gly660Val
|
|
|
XM_005267881.3:c.386G>T
|
XP_005267938.1:p.Gly129Val
|
|
|
XM_017021473.1:c.938G>T
|
XP_016876962.1:p.Gly313Val
|
|
|
XM_024449663.1:c.938G>T
|
XP_024305431.1:p.Gly313Val
|
|
|
XM_024449664.1:c.938G>T
|
XP_024305432.1:p.Gly313Val
|
|
|
XM_024449665.1:c.796+142G>T
|
XP_024305433.1:n.796+142G>T
|
|
|
XM_024449666.1:c.796+142G>T
|
XP_024305434.1:n.796+142G>T
|
|
|
NM_001377523.1:c.689-2756G>T
|
NP_001364452.1:n.689-2756G>T
|
|
|
NM_001377948.1:c.938G>T
|
NP_001364877.1:p.Gly313Val
|
|
|
NM_001377949.1:c.796+142G>T
|
NP_001364878.1:n.796+142G>T
|
|
|
NM_001377950.1:c.689-2756G>T
|
NP_001364879.1:n.689-2756G>T
|
|
|
NM_001377951.1:c.191-2756G>T
|
NP_001364880.1:n.191-2756G>T
|
|
|
NM_020366.4:c.2012G>T
MANE Select
|
NP_065099.3:p.Gly671Val
|
|
