ENST00000700061.1:c.612G=
|
|
|
ENST00000700062.1:c.612G=
|
|
|
ENST00000700065.1:n.2528G=
|
|
|
ENST00000700066.1:c.2032G=
|
ENSP00000514780.1:p.Val678=
|
|
ENST00000281513.10:c.2515G=
MANE Select
|
ENSP00000281513.5:p.Val839=
|
|
ENST00000281513.9:c.2515G=
|
ENSP00000281513.5:p.Val839=
|
|
ENST00000441755.5:c.16G=
|
ENSP00000396501.1:p.Val6=
|
|
ENST00000442506.5:c.18G=
|
|
|
NM_015909.3:c.2515G=
|
NP_056993.2:p.Val839=
|
|
NR_052013.2:n.2559G=
|
|
|
XM_011510357.1:c.2386G=
|
XP_011508659.1:p.Val796=
|
|
XM_011510358.1:c.2515G=
|
XP_011508660.1:p.Val839=
|
|
XM_011510359.1:c.1876G=
|
XP_011508661.1:p.Val626=
|
|
XM_011510360.1:c.316G=
|
XP_011508662.1:p.Val106=
|
|
XM_011510361.1:c.307G=
|
XP_011508663.1:p.Val103=
|
|
XM_011510357.2:c.2386G=
|
XP_011508659.1:p.Val796=
|
|
XM_011510358.2:c.2515G=
|
XP_011508660.1:p.Val839=
|
|
XM_011510360.2:c.316G=
|
XP_011508662.1:p.Val106=
|
|
XM_011510361.2:c.307G=
|
XP_011508663.1:p.Val103=
|
|
XM_017004317.1:c.2515G=
|
XP_016859806.1:p.Val839=
|
|
XM_024452961.1:c.1876G=
|
XP_024308729.1:p.Val626=
|
|
NM_015909.4:c.2515G=
MANE Select
|
NP_056993.2:p.Val839=
|
|
NR_052013.3:n.2545G=
|
|
|