ENST00000360215.3:c.*862G>T
MANE Select
|
ENSP00000353346.1:n.*862G>T
|
|
ENST00000496656.2:n.578+4007G>T
|
|
|
ENST00000651132.1:c.*862G>T
|
ENSP00000498322.1:n.*862G>T
|
|
ENST00000651676.1:c.*16+4364G>T
|
ENSP00000498699.1:n.*16+4364G>T
|
|
ENST00000651994.1:c.*942G>T
|
ENSP00000498310.1:n.*942G>T
|
|
ENST00000652718.1:c.508+4364G>T
|
ENSP00000498866.1:n.508+4364G>T
|
|
ENST00000360215.2:c.*862G>T
|
ENSP00000353346.1:n.*862G>T
|
|
ENST00000496656.1:n.812+4007G>T
|
|
|
NM_182548.3:c.*862G>T
|
NP_872354.1:n.*862G>T
|
|
NM_182548.4:c.*862G>T
MANE Select
|
NP_872354.1:n.*862G>T
|
|