ENST00000336411.7:c.737C>G
|
ENSP00000337915.3:p.Thr246Arg
|
|
ENST00000651162.1:n.172C>G
|
|
|
ENST00000651514.1:c.737C>G
MANE Select
|
ENSP00000498939.1:p.Thr246Arg
|
|
ENST00000651783.1:c.278C>G
|
ENSP00000498924.1:p.Thr93Arg
|
|
ENST00000652018.1:c.590C>G
|
ENSP00000498733.1:p.Thr197Arg
|
|
ENST00000336411.6:c.737C>G
|
ENSP00000337915.2:p.Thr246Arg
|
|
ENST00000354593.6:c.287C>G
|
ENSP00000346607.2:p.Thr96Arg
|
|
NM_001202855.2:c.734C>G
|
NP_001189784.1:p.Thr245Arg
|
|
NM_017460.5:c.737C>G
|
NP_059488.2:p.Thr246Arg
|
|
XM_011515841.1:c.737C>G
|
XP_011514143.1:p.Thr246Arg
|
|
XM_011515842.1:c.734C>G
|
XP_011514144.1:p.Thr245Arg
|
|
NM_017460.6:c.737C>G
MANE Select
|
NP_059488.2:p.Thr246Arg
|
|
NM_001202855.3:c.734C>G
|
NP_001189784.1:p.Thr245Arg
|
|