ENST00000282516.13:c.6439G>A
MANE Select
|
ENSP00000282516.8:p.Val2147Ile
|
|
ENST00000652901.1:c.6439G>A
|
ENSP00000499536.1:p.Val2147Ile
|
|
ENST00000282516.12:c.6439G>A
|
ENSP00000282516.8:p.Val2147Ile
|
|
ENST00000448238.2:c.6439G>A
|
ENSP00000406266.2:p.Val2147Ile
|
|
ENST00000621733.1:c.1-19040G>A
|
ENSP00000480694.1:n.1-19040G>A
|
|
NM_015384.4:c.6439G>A
|
NP_056199.2:p.Val2147Ile
|
|
NM_133433.3:c.6439G>A
|
NP_597677.2:p.Val2147Ile
|
|
XM_005248280.2:c.6439G>A
|
XP_005248337.1:p.Val2147Ile
|
|
XM_005248282.3:c.5695G>A
|
XP_005248339.2:p.Val1899Ile
|
|
XM_006714467.2:c.6439G>A
|
XP_006714530.1:p.Val2147Ile
|
|
XM_006714468.1:c.6241G>A
|
XP_006714531.1:p.Val2081Ile
|
|
XM_011514014.1:c.6058G>A
|
XP_011512316.1:p.Val2020Ile
|
|
XM_011514015.1:c.6439G>A
|
XP_011512317.1:p.Val2147Ile
|
|
XM_005248280.3:c.6439G>A
|
XP_005248337.1:p.Val2147Ile
|
|
XM_005248282.5:c.5779G>A
|
XP_005248339.3:p.Val1927Ile
|
|
XM_006714468.2:c.6241G>A
|
XP_006714531.1:p.Val2081Ile
|
|
XM_017009329.1:c.6439G>A
|
XP_016864818.1:p.Val2147Ile
|
|
XM_017009330.2:c.4822G>A
|
XP_016864819.1:p.Val1608Ile
|
|
XM_017009331.1:c.4813G>A
|
XP_016864820.1:p.Val1605Ile
|
|
NM_133433.4:c.6439G>A
MANE Select
|
NP_597677.2:p.Val2147Ile
|
|
NM_015384.5:c.6439G>A
|
NP_056199.2:p.Val2147Ile
|
|