ENST00000696142.1:c.*207G>C
|
ENSP00000512434.1:n.*207G>C
|
|
ENST00000696143.1:c.666G>C
|
ENSP00000512435.1:n.666G>C
|
|
ENST00000696153.1:c.641G>C
|
ENSP00000512444.1:p.Arg214Thr
|
|
ENST00000256474.3:c.530G>C
MANE Select
|
ENSP00000256474.3:p.Arg177Thr
|
|
ENST00000256474.2:c.530G>C
|
ENSP00000256474.2:p.Arg177Thr
|
|
ENST00000345392.2:c.407G>C
|
ENSP00000344757.2:p.Arg136Thr
|
|
ENST00000477538.1:n.666G>C
|
|
|
NM_000551.3:c.530G>C , LRG_322t1:c.530G>C
|
NP_000542.1:p.Arg177Thr
|
|
NM_198156.2:c.407G>C
|
NP_937799.1:p.Arg136Thr
|
|
NM_001354723.1:c.*84G>C
|
NP_001341652.1:n.*84G>C
|
|
NM_000551.4:c.530G>C
MANE Select
|
NP_000542.1:p.Arg177Thr
|
|
NM_001354723.2:c.*84G>C
|
NP_001341652.1:n.*84G>C
|
|
NM_198156.3:c.407G>C
|
NP_937799.1:p.Arg136Thr
|
|