ENST00000463045.3:c.55T=
|
ENSP00000481376.2:p.Leu19=
|
|
ENST00000491274.6:c.184T=
|
ENSP00000480482.2:p.Leu62=
|
|
ENST00000375499.8:c.226T=
MANE Select
|
ENSP00000364649.3:p.Leu76=
|
|
ENST00000375499.7:c.226T=
|
ENSP00000364649.3:p.Leu76=
|
|
ENST00000463045.2:c.55T=
|
ENSP00000481376.1:p.Leu19=
|
|
ENST00000466613.2:n.238T=
|
|
|
ENST00000475506.1:n.143T=
|
|
|
ENST00000485515.5:n.214T=
|
|
|
ENST00000491274.5:c.184T=
|
ENSP00000480482.1:p.Leu62=
|
|
NM_003000.2:c.226T= , LRG_316t1:c.226T=
|
NP_002991.2:p.Leu76=
|
|
NM_003000.3:c.226T=
MANE Select
|
NP_002991.2:p.Leu76=
|
|