ENST00000326003.7:c.775G=
MANE Select
|
ENSP00000314151.1:p.Ala259=
|
|
ENST00000326003.6:c.775G=
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ENSP00000314151.1:p.Ala259=
|
|
ENST00000360617.7:c.1217G=
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ENSP00000353829.2:n.1217G=
|
|
ENST00000422986.6:c.*431G=
|
ENSP00000393628.2:n.*431G=
|
|
ENST00000595392.5:c.*276G=
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ENSP00000468912.1:n.*276G=
|
|
ENST00000595952.5:c.646G=
|
ENSP00000471155.1:p.Ala216=
|
|
ENST00000596333.1:n.953G=
|
|
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ENST00000598145.1:c.777G=
|
|
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ENST00000601349.5:n.2054G=
|
|
|
ENST00000601812.1:n.1207G=
|
|
|
ENST00000617027.4:c.652G=
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ENSP00000483513.1:p.Ala218=
|
|
NM_001030047.1:c.*500G=
|
NP_001025218.1:n.*500G=
|
|
NM_001030048.1:c.646G=
|
NP_001025219.1:p.Ala216=
|
|
NM_001648.2:c.775G=
MANE Select
|
NP_001639.1:p.Ala259=
|
|
XM_011526923.1:c.793G=
|
XP_011525225.1:p.Ala265=
|
|
XR_935817.1:n.1324+862G=
|
|
|