ENST00000298139.7:c.3446A>T
MANE Select
|
ENSP00000298139.5:p.Glu1149Val
|
|
ENST00000650667.1:c.*3060A>T
|
ENSP00000498593.1:n.*3060A>T
|
|
ENST00000298139.5:c.3446A>T
|
ENSP00000298139.5:p.Glu1149Val
|
|
ENST00000521620.5:n.2079A>T
|
|
|
NM_000553.4:c.3446A>T , LRG_524t1:c.3446A>T
|
NP_000544.2:p.Glu1149Val
|
|
XM_011544639.1:c.3365A>T
|
XP_011542941.1:p.Glu1122Val
|
|
XM_011544640.1:c.1847A>T
|
XP_011542942.1:p.Glu616Val
|
|
XR_949470.1:n.3719A>T
|
|
|
XR_949471.1:n.3719A>T
|
|
|
XR_949472.1:n.3719A>T
|
|
|
XR_949643.1:n.614+1393T>A
|
|
|
NM_000553.5:c.3446A>T
|
NP_000544.2:p.Glu1149Val
|
|
XM_011544639.3:c.3365A>T
|
XP_011542941.1:p.Glu1122Val
|
|
XM_024447265.1:c.3236A>T
|
XP_024303033.1:p.Glu1079Val
|
|
XR_949470.3:n.3747A>T
|
|
|
XR_949471.3:n.3747A>T
|
|
|
XR_949472.3:n.3747A>T
|
|
|
NM_000553.6:c.3446A>T
MANE Select
|
NP_000544.2:p.Glu1149Val
|
|