ENST00000439388.6:c.774G>T
MANE Select
|
ENSP00000403084.1:p.Gln258His
|
|
ENST00000298628.6:c.774G>T
|
ENSP00000298628.5:p.Gln258His
|
|
ENST00000371867.5:c.507G>T
|
ENSP00000360933.1:p.Gln169His
|
|
ENST00000371872.8:c.774G>T
|
ENSP00000360938.4:p.Gln258His
|
|
ENST00000422262.6:c.-67G>T
|
ENSP00000415537.3:n.-67G>T
|
|
ENST00000427237.6:c.774G>T
|
ENSP00000394210.2:p.Gln258His
|
|
ENST00000439388.5:c.774G>T
|
ENSP00000403084.1:p.Gln258His
|
|
ENST00000616662.4:c.774G>T
|
ENSP00000484683.1:p.Gln258His
|
|
NM_001134707.1:c.774G>T
|
NP_001128179.1:p.Gln258His
|
|
NM_007101.3:c.774G>T
|
NP_009032.2:p.Gln258His
|
|
XM_006716990.2:c.774G>T
|
XP_006717053.1:p.Gln258His
|
|
XM_011518333.1:c.774G>T
|
XP_011516635.1:p.Gln258His
|
|
XR_929726.1:n.941G>T
|
|
|
XR_929727.1:n.941G>T
|
|
|
XR_929728.1:n.941G>T
|
|
|
XM_017014367.1:c.774G>T
|
XP_016869856.1:p.Gln258His
|
|
XM_017014368.1:c.774G>T
|
XP_016869857.1:p.Gln258His
|
|
XR_001746213.1:n.1070G>T
|
|
|
XR_001746214.1:n.2253G>T
|
|
|
XR_001746215.1:n.1072G>T
|
|
|
XR_001746216.1:n.1070G>T
|
|
|
XR_001746217.1:n.1070G>T
|
|
|
XR_001746218.1:n.1070G>T
|
|
|
XR_929726.2:n.941G>T
|
|
|
NM_001134707.2:c.774G>T
MANE Select
|
NP_001128179.1:p.Gln258His
|
|
NM_007101.4:c.774G>T
|
NP_009032.2:p.Gln258His
|
|