ENST00000635540.2:c.*209A>T
|
ENSP00000489185.1:n.*209A>T
|
|
ENST00000399799.3:c.3574A>T
MANE Select
|
ENSP00000382697.1:p.Ile1192Phe
|
|
ENST00000399799.2:c.3574A>T
|
ENSP00000382697.1:p.Ile1192Phe
|
|
ENST00000584687.1:n.284A>T
|
|
|
ENST00000635540.1:c.*209A>T
|
ENSP00000489185.1:n.*209A>T
|
|
NM_005406.2:c.3574A>T
|
NP_005397.1:p.Ile1192Phe
|
|
XM_011526136.1:c.3652A>T
|
XP_011524438.1:p.Ile1218Phe
|
|
XM_011526137.1:c.2185A>T
|
XP_011524439.1:p.Ile729Phe
|
|
XM_011526137.3:c.2185A>T
|
XP_011524439.1:p.Ile729Phe
|
|
NM_005406.3:c.3574A>T
MANE Select
|
NP_005397.1:p.Ile1192Phe
|
|