ENST00000696142.1:c.*177G=
|
ENSP00000512434.1:n.*177G=
|
|
ENST00000696143.1:c.636G=
|
ENSP00000512435.1:n.636G=
|
|
ENST00000696153.1:c.611G=
|
ENSP00000512444.1:p.Arg204=
|
|
ENST00000256474.3:c.500G=
MANE Select
|
ENSP00000256474.3:p.Arg167=
|
|
ENST00000256474.2:c.500G=
|
ENSP00000256474.2:p.Arg167=
|
|
ENST00000345392.2:c.377G=
|
ENSP00000344757.2:p.Arg126=
|
|
ENST00000477538.1:n.636G=
|
|
|
NM_000551.3:c.500G= , LRG_322t1:c.500G=
|
NP_000542.1:p.Arg167=
|
|
NM_198156.2:c.377G=
|
NP_937799.1:p.Arg126=
|
|
NM_001354723.1:c.*54G=
|
NP_001341652.1:n.*54G=
|
|
NM_000551.4:c.500G=
MANE Select
|
NP_000542.1:p.Arg167=
|
|
NM_001354723.2:c.*54G=
|
NP_001341652.1:n.*54G=
|
|
NM_198156.3:c.377G=
|
NP_937799.1:p.Arg126=
|
|