ENST00000298139.7:c.3497A>T
MANE Select
|
ENSP00000298139.5:p.Lys1166Ile
|
|
ENST00000650667.1:c.*3111A>T
|
ENSP00000498593.1:n.*3111A>T
|
|
ENST00000298139.5:c.3497A>T
|
ENSP00000298139.5:p.Lys1166Ile
|
|
ENST00000521620.5:n.2130A>T
|
|
|
NM_000553.4:c.3497A>T , LRG_524t1:c.3497A>T
|
NP_000544.2:p.Lys1166Ile
|
|
XM_011544639.1:c.3416A>T
|
XP_011542941.1:p.Lys1139Ile
|
|
XM_011544640.1:c.1898A>T
|
XP_011542942.1:p.Lys633Ile
|
|
XR_949470.1:n.3770A>T
|
|
|
XR_949471.1:n.3770A>T
|
|
|
XR_949472.1:n.3770A>T
|
|
|
XR_949643.1:n.614+1107T>A
|
|
|
NM_000553.5:c.3497A>T
|
NP_000544.2:p.Lys1166Ile
|
|
XM_011544639.3:c.3416A>T
|
XP_011542941.1:p.Lys1139Ile
|
|
XM_024447265.1:c.3287A>T
|
XP_024303033.1:p.Lys1096Ile
|
|
XR_949470.3:n.3798A>T
|
|
|
XR_949471.3:n.3798A>T
|
|
|
XR_949472.3:n.3798A>T
|
|
|
NM_000553.6:c.3497A>T
MANE Select
|
NP_000544.2:p.Lys1166Ile
|
|