ENST00000682565.1:c.11710C=
|
ENSP00000507671.1:p.Pro3904=
|
|
ENST00000682801.1:c.11167-772C=
|
ENSP00000507862.1:n.11167-772C=
|
|
ENST00000682859.1:c.11710C=
|
ENSP00000508222.1:p.Pro3904=
|
|
ENST00000683791.1:c.4796C=
|
|
|
ENST00000684460.1:c.8991C=
|
|
|
ENST00000684548.1:c.11710C=
|
ENSP00000507421.1:p.Pro3904=
|
|
ENST00000684590.1:c.6157C=
|
ENSP00000507376.1:p.Pro2053=
|
|
ENST00000684656.1:c.9175C=
|
|
|
ENST00000613296.6:c.12091C=
MANE Select
|
ENSP00000482968.1:p.Pro4031=
|
|
ENST00000651057.1:c.2245C=
|
ENSP00000498504.1:p.Pro749=
|
|
ENST00000651434.1:c.3447C=
|
|
|
ENST00000651750.1:c.1260+532C=
|
|
|
ENST00000652487.1:c.3262C=
|
|
|
ENST00000464408.3:n.266C=
|
|
|
ENST00000484298.5:c.11965C=
|
ENSP00000478155.1:p.Pro3989=
|
|
ENST00000613296.4:c.12091C=
|
ENSP00000482968.1:p.Pro4031=
|
|
ENST00000620466.4:n.5894C=
|
|
|
NM_015120.4:c.12094C= , LRG_741t1:c.12094C=
|
NP_055935.4:p.Pro4032=
|
|
NM_001378454.1:c.12091C=
MANE Select
|
NP_001365383.1:p.Pro4031=
|
|