ENST00000336411.7:c.1480T>G
|
ENSP00000337915.3:p.Phe494Val
|
|
ENST00000651162.1:n.822T>G
|
|
|
ENST00000651514.1:c.1387T>G
MANE Select
|
ENSP00000498939.1:p.Phe463Val
|
|
ENST00000651783.1:c.928T>G
|
ENSP00000498924.1:p.Phe310Val
|
|
ENST00000652018.1:c.1240T>G
|
ENSP00000498733.1:p.Phe414Val
|
|
ENST00000336411.6:c.1387T>G
|
ENSP00000337915.2:p.Phe463Val
|
|
ENST00000354593.6:c.937T>G
|
ENSP00000346607.2:p.Phe313Val
|
|
NM_001202855.2:c.1384T>G
|
NP_001189784.1:p.Phe462Val
|
|
NM_017460.5:c.1387T>G
|
NP_059488.2:p.Phe463Val
|
|
XM_011515841.1:c.1480T>G
|
XP_011514143.1:p.Phe494Val
|
|
XM_011515842.1:c.1477T>G
|
XP_011514144.1:p.Phe493Val
|
|
NM_017460.6:c.1387T>G
MANE Select
|
NP_059488.2:p.Phe463Val
|
|
NM_001202855.3:c.1384T>G
|
NP_001189784.1:p.Phe462Val
|
|