ENST00000336411.7:c.1439T>A
|
ENSP00000337915.3:p.Leu480His
|
|
ENST00000651162.1:n.781T>A
|
|
|
ENST00000651514.1:c.1346T>A
MANE Select
|
ENSP00000498939.1:p.Leu449His
|
|
ENST00000651783.1:c.887T>A
|
ENSP00000498924.1:p.Leu296His
|
|
ENST00000652018.1:c.1199T>A
|
ENSP00000498733.1:p.Leu400His
|
|
ENST00000336411.6:c.1346T>A
|
ENSP00000337915.2:p.Leu449His
|
|
ENST00000354593.6:c.896T>A
|
ENSP00000346607.2:p.Leu299His
|
|
NM_001202855.2:c.1343T>A
|
NP_001189784.1:p.Leu448His
|
|
NM_017460.5:c.1346T>A
|
NP_059488.2:p.Leu449His
|
|
XM_011515841.1:c.1439T>A
|
XP_011514143.1:p.Leu480His
|
|
XM_011515842.1:c.1436T>A
|
XP_011514144.1:p.Leu479His
|
|
NM_017460.6:c.1346T>A
MANE Select
|
NP_059488.2:p.Leu449His
|
|
NM_001202855.3:c.1343T>A
|
NP_001189784.1:p.Leu448His
|
|