ENST00000336411.7:c.1432T>G
|
ENSP00000337915.3:p.Phe478Val
|
|
ENST00000651162.1:n.774T>G
|
|
|
ENST00000651514.1:c.1339T>G
MANE Select
|
ENSP00000498939.1:p.Phe447Val
|
|
ENST00000651783.1:c.880T>G
|
ENSP00000498924.1:p.Phe294Val
|
|
ENST00000652018.1:c.1192T>G
|
ENSP00000498733.1:p.Phe398Val
|
|
ENST00000336411.6:c.1339T>G
|
ENSP00000337915.2:p.Phe447Val
|
|
ENST00000354593.6:c.889T>G
|
ENSP00000346607.2:p.Phe297Val
|
|
NM_001202855.2:c.1336T>G
|
NP_001189784.1:p.Phe446Val
|
|
NM_017460.5:c.1339T>G
|
NP_059488.2:p.Phe447Val
|
|
XM_011515841.1:c.1432T>G
|
XP_011514143.1:p.Phe478Val
|
|
XM_011515842.1:c.1429T>G
|
XP_011514144.1:p.Phe477Val
|
|
NM_017460.6:c.1339T>G
MANE Select
|
NP_059488.2:p.Phe447Val
|
|
NM_001202855.3:c.1336T>G
|
NP_001189784.1:p.Phe446Val
|
|