ENST00000315491.12:c.686T>A
MANE Select
|
ENSP00000320295.7:p.Val229Glu
|
|
ENST00000680788.1:n.4107T>A
|
|
|
ENST00000315491.11:c.686T>A
|
ENSP00000320295.7:p.Val229Glu
|
|
ENST00000554444.5:c.470T>A
|
ENSP00000451617.1:p.Val157Glu
|
|
ENST00000555576.5:c.277+1559T>A
|
ENSP00000452554.1:n.277+1559T>A
|
|
ENST00000555609.5:c.*771T>A
|
ENSP00000451276.1:n.*771T>A
|
|
ENST00000555810.5:c.470T>A
|
ENSP00000450538.1:p.Val157Glu
|
|
ENST00000556922.1:c.1727T>A
|
ENSP00000451560.1:p.Val576Glu
|
|
NM_001197181.1:c.470T>A
|
NP_001184110.1:p.Val157Glu
|
|
NM_006086.3:c.686T>A
|
NP_006077.2:p.Val229Glu
|
|
NM_006086.4:c.686T>A
MANE Select
|
NP_006077.2:p.Val229Glu
|
|
NM_001197181.2:c.470T>A
|
NP_001184110.1:p.Val157Glu
|
|