ENST00000696142.1:c.*204G>C
|
ENSP00000512434.1:n.*204G>C
|
|
ENST00000696143.1:c.663G>C
|
ENSP00000512435.1:n.663G>C
|
|
ENST00000696153.1:c.638G>C
|
ENSP00000512444.1:p.Arg213Thr
|
|
ENST00000256474.3:c.527G>C
MANE Select
|
ENSP00000256474.3:p.Arg176Thr
|
|
ENST00000256474.2:c.527G>C
|
ENSP00000256474.2:p.Arg176Thr
|
|
ENST00000345392.2:c.404G>C
|
ENSP00000344757.2:p.Arg135Thr
|
|
ENST00000477538.1:n.663G>C
|
|
|
NM_000551.3:c.527G>C , LRG_322t1:c.527G>C
|
NP_000542.1:p.Arg176Thr
|
|
NM_198156.2:c.404G>C
|
NP_937799.1:p.Arg135Thr
|
|
NM_001354723.1:c.*81G>C
|
NP_001341652.1:n.*81G>C
|
|
NM_000551.4:c.527G>C
MANE Select
|
NP_000542.1:p.Arg176Thr
|
|
NM_001354723.2:c.*81G>C
|
NP_001341652.1:n.*81G>C
|
|
NM_198156.3:c.404G>C
|
NP_937799.1:p.Arg135Thr
|
|