ENST00000635540.2:c.*210T>G
|
ENSP00000489185.1:n.*210T>G
|
|
ENST00000399799.3:c.3575T>G
MANE Select
|
ENSP00000382697.1:p.Ile1192Ser
|
|
ENST00000399799.2:c.3575T>G
|
ENSP00000382697.1:p.Ile1192Ser
|
|
ENST00000584687.1:n.285T>G
|
|
|
ENST00000635540.1:c.*210T>G
|
ENSP00000489185.1:n.*210T>G
|
|
NM_005406.2:c.3575T>G
|
NP_005397.1:p.Ile1192Ser
|
|
XM_011526136.1:c.3653T>G
|
XP_011524438.1:p.Ile1218Ser
|
|
XM_011526137.1:c.2186T>G
|
XP_011524439.1:p.Ile729Ser
|
|
XM_011526137.3:c.2186T>G
|
XP_011524439.1:p.Ile729Ser
|
|
NM_005406.3:c.3575T>G
MANE Select
|
NP_005397.1:p.Ile1192Ser
|
|