ENST00000326003.7:c.726G>A
MANE Select
|
ENSP00000314151.1:p.Leu242=
|
|
ENST00000326003.6:c.726G>A
|
ENSP00000314151.1:p.Leu242=
|
|
ENST00000360617.7:c.1168G>A
|
ENSP00000353829.2:n.1168G>A
|
|
ENST00000422986.6:c.*382G>A
|
ENSP00000393628.2:n.*382G>A
|
|
ENST00000595392.5:c.*227G>A
|
ENSP00000468912.1:n.*227G>A
|
|
ENST00000595952.5:c.597G>A
|
ENSP00000471155.1:p.Leu199=
|
|
ENST00000596333.1:n.904G>A
|
|
|
ENST00000598145.1:c.728G>A
|
|
|
ENST00000601349.5:n.2005G>A
|
|
|
ENST00000601812.1:n.1158G>A
|
|
|
ENST00000617027.4:c.603G>A
|
ENSP00000483513.1:p.Leu201=
|
|
NM_001030047.1:c.*451G>A
|
NP_001025218.1:n.*451G>A
|
|
NM_001030048.1:c.597G>A
|
NP_001025219.1:p.Leu199=
|
|
NM_001648.2:c.726G>A
MANE Select
|
NP_001639.1:p.Leu242=
|
|
XM_011526923.1:c.744G>A
|
XP_011525225.1:p.Leu248=
|
|
XR_935817.1:n.1324+813G>A
|
|
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