ENST00000696142.1:c.*396G>T
|
ENSP00000512434.1:n.*396G>T
|
|
ENST00000696143.1:c.855G>T
|
ENSP00000512435.1:n.855G>T
|
|
ENST00000696153.1:c.*77G>T
|
ENSP00000512444.1:n.*77G>T
|
|
ENST00000256474.3:c.*77G>T
MANE Select
|
ENSP00000256474.3:n.*77G>T
|
|
ENST00000256474.2:c.*77G>T
|
ENSP00000256474.2:n.*77G>T
|
|
ENST00000345392.2:c.*77G>T
|
ENSP00000344757.2:n.*77G>T
|
|
ENST00000477538.1:n.855G>T
|
|
|
NM_000551.3:c.*77G>T , LRG_322t1:c.*77G>T
|
NP_000542.1:n.*77G>T
|
|
NM_198156.2:c.*77G>T
|
NP_937799.1:n.*77G>T
|
|
NM_001354723.1:c.*273G>T
|
NP_001341652.1:n.*273G>T
|
|
NM_000551.4:c.*77G>T
MANE Select
|
NP_000542.1:n.*77G>T
|
|
NM_001354723.2:c.*273G>T
|
NP_001341652.1:n.*273G>T
|
|
NM_198156.3:c.*77G>T
|
NP_937799.1:n.*77G>T
|
|