ENST00000635540.2:c.*171T>A
|
ENSP00000489185.1:n.*171T>A
|
|
ENST00000399799.3:c.3536T>A
MANE Select
|
ENSP00000382697.1:p.Val1179Glu
|
|
ENST00000399799.2:c.3536T>A
|
ENSP00000382697.1:p.Val1179Glu
|
|
ENST00000584687.1:n.246T>A
|
|
|
ENST00000635540.1:c.*171T>A
|
ENSP00000489185.1:n.*171T>A
|
|
NM_005406.2:c.3536T>A
|
NP_005397.1:p.Val1179Glu
|
|
XM_011526136.1:c.3614T>A
|
XP_011524438.1:p.Val1205Glu
|
|
XM_011526137.1:c.2147T>A
|
XP_011524439.1:p.Val716Glu
|
|
XM_011526137.3:c.2147T>A
|
XP_011524439.1:p.Val716Glu
|
|
NM_005406.3:c.3536T>A
MANE Select
|
NP_005397.1:p.Val1179Glu
|
|