|
NM_032119.4:c.17613G>A
MANE Select
|
NP_115495.3:p.Gln5871=
|
|
ENST00000405460.9:c.17613G>A
MANE Select
|
ENSP00000384582.2:p.Gln5871=
|
|
NM_032119.3:c.17613G>A
|
NP_115495.3:p.Gln5871=
|
|
NR_003149.1:n.17626G>A
|
|
|
NR_003149.2:n.17629G>A
|
|
|
ENST00000405460.6:c.17613G>A
|
ENSP00000384582.2:p.Gln5871=
|
|
ENST00000425867.2:c.4596G>A
|
ENSP00000392618.2:p.Gln1532=
|
|
ENST00000425867.3:c.6567G>A
|
ENSP00000392618.3:p.Gln2189=
|
|
ENST00000503852.1:n.161G>A
|
|
|
ENST00000638510.1:n.4880G>A
|
|
|
ENST00000638990.1:c.825G>A
|
|
|
ENST00000639431.1:c.266-129585G>A
|
ENSP00000491057.1:n.266-129585G>A
|
|
ENST00000640407.1:c.4062G>A
|
ENSP00000491425.1:n.4062G>A
|
|
XM_011543675.1:c.17610G>A
|
XP_011541977.1:p.Gln5870=
|
|
XM_011543676.1:c.17532G>A
|
XP_011541978.1:p.Gln5844=
|
|
XM_011543677.1:c.14916G>A
|
XP_011541979.1:p.Gln4972=
|
|
XM_017009963.2:c.17634G>A
|
XP_016865452.1:p.Gln5878=
|
|
XM_017009964.2:c.17631G>A
|
XP_016865453.1:p.Gln5877=
|
|
XM_017009965.1:c.17631G>A
|
XP_016865454.1:p.Gln5877=
|
|
XM_017009966.2:c.17553G>A
|
XP_016865455.1:p.Gln5851=
|
|
XM_017009967.1:c.17538G>A
|
XP_016865456.1:p.Gln5846=
|
|
XM_017009968.2:c.17454G>A
|
XP_016865457.1:p.Gln5818=
|
|
XM_017009969.2:c.17634G>A
|
XP_016865458.1:p.Gln5878=
|
|
XM_017009972.1:c.10752G>A
|
XP_016865461.1:p.Gln3584=
|
|
XM_017009973.1:c.10731G>A
|
XP_016865462.1:p.Gln3577=
|