ENST00000480266.6:c.553G=
|
ENSP00000479015.1:p.Ala185=
|
|
ENST00000373203.9:c.1099G=
MANE Select
|
ENSP00000362299.4:p.Ala367=
|
|
ENST00000344849.4:c.1099G=
|
ENSP00000341917.3:p.Ala367=
|
|
ENST00000373203.8:c.1099G=
|
ENSP00000362299.4:p.Ala367=
|
|
ENST00000480266.5:c.553G=
|
ENSP00000479015.1:p.Ala185=
|
|
ENST00000486329.1:n.67G=
|
|
|
NM_000118.3:c.1099G= , LRG_589t1:c.1099G=
|
NP_000109.1:p.Ala367=
|
|
NM_001114753.2:c.1099G= , LRG_589t2:c.1099G=
|
NP_001108225.1:p.Ala367=
|
|
NM_001278138.1:c.553G=
|
NP_001265067.1:p.Ala185=
|
|
NM_001114753.3:c.1099G=
MANE Select
|
NP_001108225.1:p.Ala367=
|
|
NM_001278138.2:c.553G=
|
NP_001265067.1:p.Ala185=
|
|