ENST00000696142.1:c.*749G=
|
ENSP00000512434.1:n.*749G=
|
|
ENST00000696143.1:c.1208G=
|
ENSP00000512435.1:n.1208G=
|
|
ENST00000696153.1:c.*430G=
|
ENSP00000512444.1:n.*430G=
|
|
ENST00000256474.3:c.*430G=
MANE Select
|
ENSP00000256474.3:n.*430G=
|
|
ENST00000256474.2:c.*430G=
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ENSP00000256474.2:n.*430G=
|
|
ENST00000345392.2:c.*430G=
|
ENSP00000344757.2:n.*430G=
|
|
NM_000551.3:c.*430G= , LRG_322t1:c.*430G=
|
NP_000542.1:n.*430G=
|
|
NM_198156.2:c.*430G=
|
NP_937799.1:n.*430G=
|
|
NM_001354723.1:c.*626G=
|
NP_001341652.1:n.*626G=
|
|
NM_000551.4:c.*430G=
MANE Select
|
NP_000542.1:n.*430G=
|
|
NM_001354723.2:c.*626G=
|
NP_001341652.1:n.*626G=
|
|
NM_198156.3:c.*430G=
|
NP_937799.1:n.*430G=
|
|