ENST00000635540.2:c.*211T>G
|
ENSP00000489185.1:n.*211T>G
|
|
ENST00000399799.3:c.3576T>G
MANE Select
|
ENSP00000382697.1:p.Ile1192Met
|
|
ENST00000399799.2:c.3576T>G
|
ENSP00000382697.1:p.Ile1192Met
|
|
ENST00000584687.1:n.286T>G
|
|
|
ENST00000635540.1:c.*211T>G
|
ENSP00000489185.1:n.*211T>G
|
|
NM_005406.2:c.3576T>G
|
NP_005397.1:p.Ile1192Met
|
|
XM_011526136.1:c.3654T>G
|
XP_011524438.1:p.Ile1218Met
|
|
XM_011526137.1:c.2187T>G
|
XP_011524439.1:p.Ile729Met
|
|
XM_011526137.3:c.2187T>G
|
XP_011524439.1:p.Ile729Met
|
|
NM_005406.3:c.3576T>G
MANE Select
|
NP_005397.1:p.Ile1192Met
|
|