ENST00000328195.8:c.429C>T
MANE Select
|
ENSP00000333551.3:p.Val143=
|
|
ENST00000328195.7:c.429C>T
|
ENSP00000333551.3:p.Val143=
|
|
ENST00000518036.5:c.*281C>T
|
ENSP00000428005.1:n.*281C>T
|
|
ENST00000521631.1:n.112C>T
|
|
|
ENST00000523187.5:c.273C>T
|
ENSP00000427886.1:p.Val91=
|
|
ENST00000523358.5:c.429C>T
|
ENSP00000427778.1:p.Val143=
|
|
ENST00000523521.1:c.186C>T
|
ENSP00000429425.1:p.Val62=
|
|
NM_007198.3:c.429C>T
|
NP_009129.1:p.Val143=
|
|
NM_001349346.1:c.429C>T
|
NP_001336275.1:p.Val143=
|
|
NM_001349347.1:c.423C>T
|
NP_001336276.1:p.Val141=
|
|
NM_001349348.1:c.273C>T
|
NP_001336277.1:p.Val91=
|
|
NM_007198.4:c.429C>T
MANE Select
|
NP_009129.1:p.Val143=
|
|
NM_001349346.2:c.429C>T
|
NP_001336275.1:p.Val143=
|
|
NM_001349347.2:c.423C>T
|
NP_001336276.1:p.Val141=
|
|
NM_001349348.2:c.273C>T
|
NP_001336277.1:p.Val91=
|
|