ENST00000700061.1:c.605G>T
|
|
|
ENST00000700062.1:c.605G>T
|
|
|
ENST00000700065.1:n.2521G>T
|
|
|
ENST00000700066.1:c.2025G>T
|
ENSP00000514780.1:p.Gln675His
|
|
ENST00000281513.10:c.2508G>T
MANE Select
|
ENSP00000281513.5:p.Gln836His
|
|
ENST00000281513.9:c.2508G>T
|
ENSP00000281513.5:p.Gln836His
|
|
ENST00000441755.5:c.9G>T
|
ENSP00000396501.1:p.Gln3His
|
|
ENST00000442506.5:c.11G>T
|
|
|
NM_015909.3:c.2508G>T
|
NP_056993.2:p.Gln836His
|
|
NR_052013.2:n.2552G>T
|
|
|
XM_011510357.1:c.2379G>T
|
XP_011508659.1:p.Gln793His
|
|
XM_011510358.1:c.2508G>T
|
XP_011508660.1:p.Gln836His
|
|
XM_011510359.1:c.1869G>T
|
XP_011508661.1:p.Gln623His
|
|
XM_011510360.1:c.309G>T
|
XP_011508662.1:p.Gln103His
|
|
XM_011510361.1:c.300G>T
|
XP_011508663.1:p.Gln100His
|
|
XM_011510357.2:c.2379G>T
|
XP_011508659.1:p.Gln793His
|
|
XM_011510358.2:c.2508G>T
|
XP_011508660.1:p.Gln836His
|
|
XM_011510360.2:c.309G>T
|
XP_011508662.1:p.Gln103His
|
|
XM_011510361.2:c.300G>T
|
XP_011508663.1:p.Gln100His
|
|
XM_017004317.1:c.2508G>T
|
XP_016859806.1:p.Gln836His
|
|
XM_024452961.1:c.1869G>T
|
XP_024308729.1:p.Gln623His
|
|
NM_015909.4:c.2508G>T
MANE Select
|
NP_056993.2:p.Gln836His
|
|
NR_052013.3:n.2538G>T
|
|
|