ENST00000696142.1:c.*205G>T
|
ENSP00000512434.1:n.*205G>T
|
|
ENST00000696143.1:c.664G>T
|
ENSP00000512435.1:n.664G>T
|
|
ENST00000696153.1:c.639G>T
|
ENSP00000512444.1:p.Arg213Ser
|
|
ENST00000256474.3:c.528G>T
MANE Select
|
ENSP00000256474.3:p.Arg176Ser
|
|
ENST00000256474.2:c.528G>T
|
ENSP00000256474.2:p.Arg176Ser
|
|
ENST00000345392.2:c.405G>T
|
ENSP00000344757.2:p.Arg135Ser
|
|
ENST00000477538.1:n.664G>T
|
|
|
NM_000551.3:c.528G>T , LRG_322t1:c.528G>T
|
NP_000542.1:p.Arg176Ser
|
|
NM_198156.2:c.405G>T
|
NP_937799.1:p.Arg135Ser
|
|
NM_001354723.1:c.*82G>T
|
NP_001341652.1:n.*82G>T
|
|
NM_000551.4:c.528G>T
MANE Select
|
NP_000542.1:p.Arg176Ser
|
|
NM_001354723.2:c.*82G>T
|
NP_001341652.1:n.*82G>T
|
|
NM_198156.3:c.405G>T
|
NP_937799.1:p.Arg135Ser
|
|