ENST00000282516.13:c.7830G=
MANE Select
|
ENSP00000282516.8:p.Val2610=
|
|
ENST00000652901.1:c.7683G=
|
ENSP00000499536.1:p.Val2561=
|
|
ENST00000282516.12:c.7830G=
|
ENSP00000282516.8:p.Val2610=
|
|
ENST00000448238.2:c.7830G=
|
ENSP00000406266.2:p.Val2610=
|
|
ENST00000513819.1:c.263+1823G=
|
ENSP00000421504.1:n.263+1823G=
|
|
ENST00000514335.1:n.1712G=
|
|
|
ENST00000621733.1:c.1-3590G=
|
ENSP00000480694.1:n.1-3590G=
|
|
NM_015384.4:c.7830G=
|
NP_056199.2:p.Val2610=
|
|
NM_133433.3:c.7830G=
|
NP_597677.2:p.Val2610=
|
|
XM_005248280.2:c.7830G=
|
XP_005248337.1:p.Val2610=
|
|
XM_005248282.3:c.7086G=
|
XP_005248339.2:p.Val2362=
|
|
XM_006714467.2:c.7683G=
|
XP_006714530.1:p.Val2561=
|
|
XM_006714468.1:c.7632G=
|
XP_006714531.1:p.Val2544=
|
|
XM_011514014.1:c.7449G=
|
XP_011512316.1:p.Val2483=
|
|
XM_005248280.3:c.7830G=
|
XP_005248337.1:p.Val2610=
|
|
XM_005248282.5:c.7170G=
|
XP_005248339.3:p.Val2390=
|
|
XM_006714468.2:c.7632G=
|
XP_006714531.1:p.Val2544=
|
|
XM_017009329.1:c.7683G=
|
XP_016864818.1:p.Val2561=
|
|
XM_017009330.2:c.6213G=
|
XP_016864819.1:p.Val2071=
|
|
XM_017009331.1:c.6204G=
|
XP_016864820.1:p.Val2068=
|
|
NM_133433.4:c.7830G=
MANE Select
|
NP_597677.2:p.Val2610=
|
|
NM_015384.5:c.7830G=
|
NP_056199.2:p.Val2610=
|
|