ENST00000463045.3:c.299T=
|
ENSP00000481376.2:p.Leu100=
|
|
ENST00000491274.6:c.428T=
|
ENSP00000480482.2:p.Leu143=
|
|
ENST00000375499.8:c.470T=
MANE Select
|
ENSP00000364649.3:p.Leu157=
|
|
ENST00000375499.7:c.470T=
|
ENSP00000364649.3:p.Leu157=
|
|
ENST00000463045.2:c.299T=
|
ENSP00000481376.1:p.Leu100=
|
|
ENST00000475506.1:n.387T=
|
|
|
ENST00000485515.5:n.404T=
|
|
|
ENST00000491274.5:c.428T=
|
ENSP00000480482.1:p.Leu143=
|
|
NM_003000.2:c.470T= , LRG_316t1:c.470T=
|
NP_002991.2:p.Leu157=
|
|
NM_003000.3:c.470T=
MANE Select
|
NP_002991.2:p.Leu157=
|
|