ENST00000392676.8:c.4251A=
MANE Select
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ENSP00000376443.2:p.Thr1417=
|
|
ENST00000392676.7:c.4251A=
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ENSP00000376443.2:p.Thr1417=
|
|
ENST00000586811.1:c.1149A=
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ENSP00000465351.1:p.Thr383=
|
|
ENST00000586995.5:c.3313A=
|
ENSP00000467251.1:n.3313A=
|
|
ENST00000588877.5:c.4251A=
|
ENSP00000467882.1:p.Thr1417=
|
|
ENST00000591234.5:c.2193A=
|
ENSP00000465766.1:n.2193A=
|
|
NM_018672.4:c.4251A=
|
NP_061142.2:p.Thr1417=
|
|
NM_172232.3:c.4251A=
|
NP_758424.1:p.Thr1417=
|
|
NM_172232.4:c.4251A=
MANE Select
|
NP_758424.1:p.Thr1417=
|
|
NM_018672.5:c.4251A=
|
NP_061142.2:p.Thr1417=
|
|