ENST00000336411.7:c.1459C>G
|
ENSP00000337915.3:p.Leu487Val
|
|
ENST00000651162.1:n.801C>G
|
|
|
ENST00000651514.1:c.1366C>G
MANE Select
|
ENSP00000498939.1:p.Leu456Val
|
|
ENST00000651783.1:c.907C>G
|
ENSP00000498924.1:p.Leu303Val
|
|
ENST00000652018.1:c.1219C>G
|
ENSP00000498733.1:p.Leu407Val
|
|
ENST00000336411.6:c.1366C>G
|
ENSP00000337915.2:p.Leu456Val
|
|
ENST00000354593.6:c.916C>G
|
ENSP00000346607.2:p.Leu306Val
|
|
NM_001202855.2:c.1363C>G
|
NP_001189784.1:p.Leu455Val
|
|
NM_017460.5:c.1366C>G
|
NP_059488.2:p.Leu456Val
|
|
XM_011515841.1:c.1459C>G
|
XP_011514143.1:p.Leu487Val
|
|
XM_011515842.1:c.1456C>G
|
XP_011514144.1:p.Leu486Val
|
|
NM_017460.6:c.1366C>G
MANE Select
|
NP_059488.2:p.Leu456Val
|
|
NM_001202855.3:c.1363C>G
|
NP_001189784.1:p.Leu455Val
|
|