ENST00000480266.6:c.*502C=
|
ENSP00000479015.1:n.*502C=
|
|
ENST00000373203.9:c.*502C=
MANE Select
|
ENSP00000362299.4:n.*502C=
|
|
ENST00000344849.4:c.*737C=
|
ENSP00000341917.3:n.*737C=
|
|
ENST00000373203.8:c.*502C=
|
ENSP00000362299.4:n.*502C=
|
|
ENST00000480266.5:c.*502C=
|
ENSP00000479015.1:n.*502C=
|
|
NM_000118.3:c.*737C= , LRG_589t1:c.*737C=
|
NP_000109.1:n.*737C=
|
|
NM_001114753.2:c.*502C= , LRG_589t2:c.*502C=
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NP_001108225.1:n.*502C=
|
|
NM_001278138.1:c.*502C=
|
NP_001265067.1:n.*502C=
|
|
NM_001114753.3:c.*502C=
MANE Select
|
NP_001108225.1:n.*502C=
|
|
NM_001278138.2:c.*502C=
|
NP_001265067.1:n.*502C=
|
|