ENST00000336411.7:c.655T>G
|
ENSP00000337915.3:p.Phe219Val
|
|
ENST00000651514.1:c.655T>G
MANE Select
|
ENSP00000498939.1:p.Phe219Val
|
|
ENST00000651783.1:c.196T>G
|
ENSP00000498924.1:p.Phe66Val
|
|
ENST00000652018.1:c.508T>G
|
ENSP00000498733.1:p.Phe170Val
|
|
ENST00000336411.6:c.655T>G
|
ENSP00000337915.2:p.Phe219Val
|
|
ENST00000354593.6:c.205T>G
|
ENSP00000346607.2:p.Phe69Val
|
|
NM_001202855.2:c.655T>G
|
NP_001189784.1:p.Phe219Val
|
|
NM_017460.5:c.655T>G
|
NP_059488.2:p.Phe219Val
|
|
XM_011515841.1:c.655T>G
|
XP_011514143.1:p.Phe219Val
|
|
XM_011515842.1:c.655T>G
|
XP_011514144.1:p.Phe219Val
|
|
NM_017460.6:c.655T>G
MANE Select
|
NP_059488.2:p.Phe219Val
|
|
NM_001202855.3:c.655T>G
|
NP_001189784.1:p.Phe219Val
|
|