ENST00000298139.7:c.4290T>A
MANE Select
|
ENSP00000298139.5:p.Leu1430=
|
|
ENST00000650667.1:c.*3904T>A
|
ENSP00000498593.1:n.*3904T>A
|
|
ENST00000651946.1:n.514T>A
|
|
|
ENST00000298139.5:c.4290T>A
|
ENSP00000298139.5:p.Leu1430=
|
|
ENST00000521620.5:n.2923T>A
|
|
|
NM_000553.4:c.4290T>A , LRG_524t1:c.4290T>A
|
NP_000544.2:p.Leu1430=
|
|
XM_011544639.1:c.4209T>A
|
XP_011542941.1:p.Leu1403=
|
|
XM_011544640.1:c.2691T>A
|
XP_011542942.1:p.Leu897=
|
|
XR_949643.1:n.88-1775A>T
|
|
|
XR_949644.1:n.88-1775A>T
|
|
|
XR_949645.1:n.88-1775A>T
|
|
|
XR_949646.1:n.88-1775A>T
|
|
|
XR_949647.1:n.701-1775A>T
|
|
|
XR_949648.1:n.603-1775A>T
|
|
|
NM_000553.5:c.4290T>A
|
NP_000544.2:p.Leu1430=
|
|
XM_011544639.3:c.4209T>A
|
XP_011542941.1:p.Leu1403=
|
|
XM_024447265.1:c.4080T>A
|
XP_024303033.1:p.Leu1360=
|
|
NM_000553.6:c.4290T>A
MANE Select
|
NP_000544.2:p.Leu1430=
|
|