ENST00000326003.7:c.633T>A
MANE Select
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ENSP00000314151.1:p.Gly211=
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ENST00000326003.6:c.633T>A
|
ENSP00000314151.1:p.Gly211=
|
|
ENST00000360617.7:c.1075T>A
|
ENSP00000353829.2:n.1075T>A
|
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ENST00000422986.6:c.*289T>A
|
ENSP00000393628.2:n.*289T>A
|
|
ENST00000595392.5:c.*134T>A
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ENSP00000468912.1:n.*134T>A
|
|
ENST00000595952.5:c.504T>A
|
ENSP00000471155.1:p.Gly168=
|
|
ENST00000596185.5:c.*741T>A
|
ENSP00000471648.1:n.*741T>A
|
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ENST00000596333.1:n.811T>A
|
|
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ENST00000598145.1:c.635T>A
|
|
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ENST00000601349.5:n.1912T>A
|
|
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ENST00000601812.1:n.1065T>A
|
|
|
ENST00000617027.4:c.510T>A
|
ENSP00000483513.1:p.Gly170=
|
|
NM_001030047.1:c.*358T>A
|
NP_001025218.1:n.*358T>A
|
|
NM_001030048.1:c.504T>A
|
NP_001025219.1:p.Gly168=
|
|
NM_001648.2:c.633T>A
MANE Select
|
NP_001639.1:p.Gly211=
|
|
XM_011526923.1:c.651T>A
|
XP_011525225.1:p.Gly217=
|
|
XM_011526924.1:c.*358T>A
|
XP_011525226.1:n.*358T>A
|
|
XR_935817.1:n.1324+720T>A
|
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