ENST00000326003.7:c.705C>G
MANE Select
|
ENSP00000314151.1:p.Ala235=
|
|
ENST00000326003.6:c.705C>G
|
ENSP00000314151.1:p.Ala235=
|
|
ENST00000360617.7:c.1147C>G
|
ENSP00000353829.2:n.1147C>G
|
|
ENST00000422986.6:c.*361C>G
|
ENSP00000393628.2:n.*361C>G
|
|
ENST00000595392.5:c.*206C>G
|
ENSP00000468912.1:n.*206C>G
|
|
ENST00000595952.5:c.576C>G
|
ENSP00000471155.1:p.Ala192=
|
|
ENST00000596333.1:n.883C>G
|
|
|
ENST00000598145.1:c.707C>G
|
|
|
ENST00000601349.5:n.1984C>G
|
|
|
ENST00000601812.1:n.1137C>G
|
|
|
ENST00000617027.4:c.582C>G
|
ENSP00000483513.1:p.Ala194=
|
|
NM_001030047.1:c.*430C>G
|
NP_001025218.1:n.*430C>G
|
|
NM_001030048.1:c.576C>G
|
NP_001025219.1:p.Ala192=
|
|
NM_001648.2:c.705C>G
MANE Select
|
NP_001639.1:p.Ala235=
|
|
XM_011526923.1:c.723C>G
|
XP_011525225.1:p.Ala241=
|
|
XR_935817.1:n.1324+792C>G
|
|
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