ENST00000336411.7:c.419G>T
|
ENSP00000337915.3:p.Gly140Val
|
|
ENST00000651514.1:c.419G>T
MANE Select
|
ENSP00000498939.1:p.Gly140Val
|
|
ENST00000651783.1:c.58-1628G>T
|
ENSP00000498924.1:n.58-1628G>T
|
|
ENST00000652018.1:c.272G>T
|
ENSP00000498733.1:p.Gly91Val
|
|
ENST00000336411.6:c.419G>T
|
ENSP00000337915.2:p.Gly140Val
|
|
ENST00000354593.6:c.72-1633G>T
|
ENSP00000346607.2:n.72-1633G>T
|
|
ENST00000415003.1:c.458G>T
|
ENSP00000397208.1:p.Gly153Val
|
|
ENST00000480043.1:n.316G>T
|
|
|
NM_001202855.2:c.419G>T
|
NP_001189784.1:p.Gly140Val
|
|
NM_017460.5:c.419G>T
|
NP_059488.2:p.Gly140Val
|
|
XM_011515841.1:c.419G>T
|
XP_011514143.1:p.Gly140Val
|
|
XM_011515842.1:c.419G>T
|
XP_011514144.1:p.Gly140Val
|
|
NM_017460.6:c.419G>T
MANE Select
|
NP_059488.2:p.Gly140Val
|
|
NM_001202855.3:c.419G>T
|
NP_001189784.1:p.Gly140Val
|
|