ENST00000635540.2:c.*211T>C
|
ENSP00000489185.1:n.*211T>C
|
|
ENST00000399799.3:c.3576T>C
MANE Select
|
ENSP00000382697.1:p.Ile1192=
|
|
ENST00000399799.2:c.3576T>C
|
ENSP00000382697.1:p.Ile1192=
|
|
ENST00000584687.1:n.286T>C
|
|
|
ENST00000635540.1:c.*211T>C
|
ENSP00000489185.1:n.*211T>C
|
|
NM_005406.2:c.3576T>C
|
NP_005397.1:p.Ile1192=
|
|
XM_011526136.1:c.3654T>C
|
XP_011524438.1:p.Ile1218=
|
|
XM_011526137.1:c.2187T>C
|
XP_011524439.1:p.Ile729=
|
|
XM_011526137.3:c.2187T>C
|
XP_011524439.1:p.Ile729=
|
|
NM_005406.3:c.3576T>C
MANE Select
|
NP_005397.1:p.Ile1192=
|
|