ENST00000298139.7:c.3696C>G
MANE Select
|
ENSP00000298139.5:p.Leu1232=
|
|
ENST00000650667.1:c.*3310C>G
|
ENSP00000498593.1:n.*3310C>G
|
|
ENST00000298139.5:c.3696C>G
|
ENSP00000298139.5:p.Leu1232=
|
|
ENST00000521620.5:n.2329C>G
|
|
|
NM_000553.4:c.3696C>G , LRG_524t1:c.3696C>G
|
NP_000544.2:p.Leu1232=
|
|
XM_011544639.1:c.3615C>G
|
XP_011542941.1:p.Leu1205=
|
|
XM_011544640.1:c.2097C>G
|
XP_011542942.1:p.Leu699=
|
|
XR_949470.1:n.3969C>G
|
|
|
XR_949471.1:n.3969C>G
|
|
|
XR_949472.1:n.3969C>G
|
|
|
XR_949643.1:n.457-5967G>C
|
|
|
XR_949644.1:n.381-5967G>C
|
|
|
XR_949647.1:n.1070-5967G>C
|
|
|
XR_949648.1:n.972-5967G>C
|
|
|
NM_000553.5:c.3696C>G
|
NP_000544.2:p.Leu1232=
|
|
XM_011544639.3:c.3615C>G
|
XP_011542941.1:p.Leu1205=
|
|
XM_024447265.1:c.3486C>G
|
XP_024303033.1:p.Leu1162=
|
|
XR_949470.3:n.3997C>G
|
|
|
XR_949471.3:n.3997C>G
|
|
|
XR_949472.3:n.3997C>G
|
|
|
NM_000553.6:c.3696C>G
MANE Select
|
NP_000544.2:p.Leu1232=
|
|