ENST00000336411.7:c.1426A>G
|
ENSP00000337915.3:p.Met476Val
|
|
ENST00000651162.1:n.768A>G
|
|
|
ENST00000651514.1:c.1333A>G
MANE Select
|
ENSP00000498939.1:p.Met445Val
|
|
ENST00000651783.1:c.874A>G
|
ENSP00000498924.1:p.Met292Val
|
|
ENST00000652018.1:c.1186A>G
|
ENSP00000498733.1:p.Met396Val
|
|
ENST00000336411.6:c.1333A>G
|
ENSP00000337915.2:p.Met445Val
|
|
ENST00000354593.6:c.883A>G
|
ENSP00000346607.2:p.Met295Val
|
|
NM_001202855.2:c.1330A>G
|
NP_001189784.1:p.Met444Val
|
|
NM_017460.5:c.1333A>G
|
NP_059488.2:p.Met445Val
|
|
XM_011515841.1:c.1426A>G
|
XP_011514143.1:p.Met476Val
|
|
XM_011515842.1:c.1423A>G
|
XP_011514144.1:p.Met475Val
|
|
NM_017460.6:c.1333A>G
MANE Select
|
NP_059488.2:p.Met445Val
|
|
NM_001202855.3:c.1330A>G
|
NP_001189784.1:p.Met444Val
|
|