ENST00000326003.7:c.721T>A
MANE Select
|
ENSP00000314151.1:p.Ser241Thr
|
|
ENST00000326003.6:c.721T>A
|
ENSP00000314151.1:p.Ser241Thr
|
|
ENST00000360617.7:c.1163T>A
|
ENSP00000353829.2:n.1163T>A
|
|
ENST00000422986.6:c.*377T>A
|
ENSP00000393628.2:n.*377T>A
|
|
ENST00000595392.5:c.*222T>A
|
ENSP00000468912.1:n.*222T>A
|
|
ENST00000595952.5:c.592T>A
|
ENSP00000471155.1:p.Ser198Thr
|
|
ENST00000596333.1:n.899T>A
|
|
|
ENST00000598145.1:c.723T>A
|
|
|
ENST00000601349.5:n.2000T>A
|
|
|
ENST00000601812.1:n.1153T>A
|
|
|
ENST00000617027.4:c.598T>A
|
ENSP00000483513.1:p.Ser200Thr
|
|
NM_001030047.1:c.*446T>A
|
NP_001025218.1:n.*446T>A
|
|
NM_001030048.1:c.592T>A
|
NP_001025219.1:p.Ser198Thr
|
|
NM_001648.2:c.721T>A
MANE Select
|
NP_001639.1:p.Ser241Thr
|
|
XM_011526923.1:c.739T>A
|
XP_011525225.1:p.Ser247Thr
|
|
XR_935817.1:n.1324+808T>A
|
|
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