ENST00000328195.8:c.423T>C
MANE Select
|
ENSP00000333551.3:p.Val141=
|
|
ENST00000328195.7:c.423T>C
|
ENSP00000333551.3:p.Val141=
|
|
ENST00000518036.5:c.*275T>C
|
ENSP00000428005.1:n.*275T>C
|
|
ENST00000521631.1:n.106T>C
|
|
|
ENST00000523187.5:c.267T>C
|
ENSP00000427886.1:p.Val89=
|
|
ENST00000523358.5:c.423T>C
|
ENSP00000427778.1:p.Val141=
|
|
ENST00000523521.1:c.180T>C
|
ENSP00000429425.1:p.Val60=
|
|
NM_007198.3:c.423T>C
|
NP_009129.1:p.Val141=
|
|
NM_001349346.1:c.423T>C
|
NP_001336275.1:p.Val141=
|
|
NM_001349347.1:c.417T>C
|
NP_001336276.1:p.Val139=
|
|
NM_001349348.1:c.267T>C
|
NP_001336277.1:p.Val89=
|
|
NM_007198.4:c.423T>C
MANE Select
|
NP_009129.1:p.Val141=
|
|
NM_001349346.2:c.423T>C
|
NP_001336275.1:p.Val141=
|
|
NM_001349347.2:c.417T>C
|
NP_001336276.1:p.Val139=
|
|
NM_001349348.2:c.267T>C
|
NP_001336277.1:p.Val89=
|
|