ENST00000336411.7:c.1497T>A
|
ENSP00000337915.3:p.Cys499Ter
|
|
ENST00000651162.1:n.839T>A
|
|
|
ENST00000651514.1:c.1404T>A
MANE Select
|
ENSP00000498939.1:p.Cys468Ter
|
|
ENST00000651783.1:c.945T>A
|
ENSP00000498924.1:p.Cys315Ter
|
|
ENST00000652018.1:c.1257T>A
|
ENSP00000498733.1:p.Cys419Ter
|
|
ENST00000336411.6:c.1404T>A
|
ENSP00000337915.2:p.Cys468Ter
|
|
ENST00000354593.6:c.954T>A
|
ENSP00000346607.2:p.Cys318Ter
|
|
NM_001202855.2:c.1401T>A
|
NP_001189784.1:p.Cys467Ter
|
|
NM_017460.5:c.1404T>A
|
NP_059488.2:p.Cys468Ter
|
|
XM_011515841.1:c.1497T>A
|
XP_011514143.1:p.Cys499Ter
|
|
XM_011515842.1:c.1494T>A
|
XP_011514144.1:p.Cys498Ter
|
|
NM_017460.6:c.1404T>A
MANE Select
|
NP_059488.2:p.Cys468Ter
|
|
NM_001202855.3:c.1401T>A
|
NP_001189784.1:p.Cys467Ter
|
|