ENST00000696142.1:c.*185G>T
|
ENSP00000512434.1:n.*185G>T
|
|
ENST00000696143.1:c.644G>T
|
ENSP00000512435.1:n.644G>T
|
|
ENST00000696153.1:c.619G>T
|
ENSP00000512444.1:p.Val207Phe
|
|
ENST00000256474.3:c.508G>T
MANE Select
|
ENSP00000256474.3:p.Val170Phe
|
|
ENST00000256474.2:c.508G>T
|
ENSP00000256474.2:p.Val170Phe
|
|
ENST00000345392.2:c.385G>T
|
ENSP00000344757.2:p.Val129Phe
|
|
ENST00000477538.1:n.644G>T
|
|
|
NM_000551.3:c.508G>T , LRG_322t1:c.508G>T
|
NP_000542.1:p.Val170Phe
|
|
NM_198156.2:c.385G>T
|
NP_937799.1:p.Val129Phe
|
|
NM_001354723.1:c.*62G>T
|
NP_001341652.1:n.*62G>T
|
|
NM_000551.4:c.508G>T
MANE Select
|
NP_000542.1:p.Val170Phe
|
|
NM_001354723.2:c.*62G>T
|
NP_001341652.1:n.*62G>T
|
|
NM_198156.3:c.385G>T
|
NP_937799.1:p.Val129Phe
|
|