ENST00000336411.7:c.1442T=
|
ENSP00000337915.3:p.Met481=
|
|
ENST00000651162.1:n.784T=
|
|
|
ENST00000651514.1:c.1349T=
MANE Select
|
ENSP00000498939.1:p.Met450=
|
|
ENST00000651783.1:c.890T=
|
ENSP00000498924.1:p.Met297=
|
|
ENST00000652018.1:c.1202T=
|
ENSP00000498733.1:p.Met401=
|
|
ENST00000336411.6:c.1349T=
|
ENSP00000337915.2:p.Met450=
|
|
ENST00000354593.6:c.899T=
|
ENSP00000346607.2:p.Met300=
|
|
NM_001202855.2:c.1346T=
|
NP_001189784.1:p.Met449=
|
|
NM_017460.5:c.1349T=
|
NP_059488.2:p.Met450=
|
|
XM_011515841.1:c.1442T=
|
XP_011514143.1:p.Met481=
|
|
XM_011515842.1:c.1439T=
|
XP_011514144.1:p.Met480=
|
|
NM_017460.6:c.1349T=
MANE Select
|
NP_059488.2:p.Met450=
|
|
NM_001202855.3:c.1346T=
|
NP_001189784.1:p.Met449=
|
|